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Symptoms » Male sexual symptoms » Glossary
 

Glossary for Male sexual symptoms

Medical terms related to Male sexual symptoms or mentioned in this section include:

  • 11q Partial Trisomy: A very rare genetic disorder caused by a duplication of part of chromosome 11q. The characteristic symptoms of the disorder are delayed growth before and after birth, mental retardation (varying severity) and skull and facial defects. The type and severity of symptoms that can occur are variable.
  • 46,XX testicular DSD: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
  • 46,XX testicular disorder of sex development: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
  • 49,XXXXY syndrome: A rare sex chromosome abnormality where there are three extra copies of the X chromosome.
  • ACPS III: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • Abidi X-linked mental retardation syndrome: A rare genetic disorder characterized by a number of physical abnormalities
  • Ablepharon macrostomia syndrome: A rare disorder involving a number of mainly physical abnormalities.
  • Acro-pectoro-renal field defect: A very rare genetic syndrome characterized by abnormalities of the genital and urinary systems as well as the absence of chest muscles at birth.
  • Acrocephalopolydactyly -- Cardiac Disease -- Ear, Skin and Lower Limb Defects: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • Acrocephalopolysyndactyly type III: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • Acrofacial dysostosis Catania form: One of a group of disorders characterized by defective limb and facial development. The Catania form is very rare.
  • Acromegaly: An abnormal enlargement of the limbs due to increased secretion of growth hormone after the cessation of puberty
  • Acute epididymitis:
  • Acute herpes-like penile ulcers: formation of vesicles similar to the presentation in herpes
  • Acute prostate blockage like symptoms: conditions which cause acute symptoms similar to that when there is a blockage to prostate secretions
  • Acute prostate pain symptoms: conditions which cause acute pain similar to that of pain due to a prostatic pathology
  • Acute prostate symptoms: acute symptoms related to the prostate includes painful micturition, hestiatancy and frequency of micturition
  • Acute prostate-related urinary dribbling: weak urinary stream
  • Acute prostate-related urinary symptoms: Symptoms include urinary frequency, urgency, urgency incontinence, voiding at night (nocturia), weak urinary stream, hesitency (needing to wait for the stream to begin), intermittency (when the stream starts and stops intermittently), straining to void, dysuria (burning sensation in the urethra), and dribbling
  • Acute prostate-related weak urinary stream: weak urinary stream
  • Acute prostatitis: An acute condition which affects the prostate which is the result of infammation
  • Acute testicular pain in children: Acute testicular pain in children is the sudden appearance of pain or discomfort in the testicle or testicles of a child.
  • Acute torsion of testis:
  • Adrenoleukodystrophy: A rare hereditary metabolic disease that only occurs in male children and is characterized by adrenal atrophy and extensive cerebral demyelination causing progressive loss of mental functioning, aphasia, apraxia and sometimes blindness. The patient usually dies within 5 years.
  • Agnathia-holoprosencephaly-situs inversus: A very rare disorder characterized by a small or absent jaw, developmental brain defect and internal organs situated on the wrong side of the body (situs inversus). The severity and range of symptoms is variable.
  • Al Awadi syndrome: A rare syndrome characterized primarily by severe malformations involving the limbs and pelvis.
  • Al Awadi-Raas-Rothschild syndrome: A rare syndrome characterized primarily by severe malformations involving the limbs and pelvis. The exact type and severity of symptoms is variable. Most cases appear to occur in cases where the parents were related.
  • Alcock syndrome: A nerve disorder which causes pain in the pelvic, genital and perianal areas.
  • Alcohol abuse: Excessive alcohol as a symptom of other conditions
  • Andrade's syndrome: An inherited condition characterized by deposits of an abnormal protein called amyloid in various parts of the body including organs. The condition mainly involves neurological symptoms.
  • Androgen Insensitivity Syndrome: Females with male XY genetics but inability to respond to testosterone.
  • Androgen insensitivity syndrome, partial: A rare inherited condition where males are partially insensitive to the male hormones which results in varying degrees of feminization. The effect of the condition can range from the presence of normal female sexual characteristics to normal male sexual characteristics or a combination of both.
  • Andropause: A symptomatic decline in male androgens that may occur as men age.
  • Aniridia -- absent patella: A rare genetic condition characterized by an abnormal or missing kneecap as well as the absence of the iris of the eye.
  • Anophthalmia/microphthalmia -- esophageal atresia: A rare disorder characterized by esophageal and genital defects as well as absent or very small eyes.
  • Anorchidia: A rare birth defect where the testes are absent. The testes may regress at any stage of fetal development. The stage of fetal growth at which the testes regress will affect the presentation of the disorder at birth. The presentation at birth may range from varying degrees of genital ambiguity with streak gonads.
  • Aromatase deficiency: A congenital deficiency of the enzyme called aromatase which is needed to convert androgens to estrogens.
  • Arthrogryposis multiplex congenita, distal, X-linked: A rare condition characterized by the presence of contractures at birth as well as various other anomalies. The condition is X-linked.
  • Aspartylglucosaminidase deficiency: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
  • Aspartylglucosaminuria: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
  • Aspartylglycosaminuria: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
  • Atherosclerosis: A condition which is a form of arteriosclerosis where atheromas are caused by the aggregation of cholesterol and lipids
  • Autonomic dysfunction: disease or malfunction of the autonomic nervous system.
  • Autonomic neuropathy: A condition which is characterized by a functional disturbance or pathological change in the autonomic nervous system
  • Bacterial prostatitis: Bacterial prostatitis is a bacterial inflammation of the prostate gland, in men.
  • Balanitis: Inflammation of the glans (or head) of the penis.
  • Balanitis xerotica obliterans: A chronic, progressive skin condition involving sclerosis and atrophic processes of the penis.
  • Bannayan-Zonana syndrome: A rare genetic disorder characterized by macrocephaly, intestinal polyposis, pigmentation of penis and benign tumor-like growths.
  • Bardet-Biedl Syndrome: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities.
  • Bardet-Biedl syndrome, type 1: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 1 is caused by a defect in chromosome 11q13.
  • Bardet-Biedl syndrome, type 10: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 10 is caused by a defect in chromosome 12q.
  • Bardet-Biedl syndrome, type 11: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 11 is caused by a defect in chromosome 9q33.1.
  • Bardet-Biedl syndrome, type 12: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 12 is caused by a defect in chromosome 4q27.
  • Bardet-Biedl syndrome, type 2: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 2 is caused by a defect in chromosome 16q21.
  • Bardet-Biedl syndrome, type 3: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 3 is caused by a defect in chromosome 3p12-q13.
  • Bardet-Biedl syndrome, type 4: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 4 is caused by a defect in chromosome 15q22.3.
  • Bardet-Biedl syndrome, type 5: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 5 is caused by a defect in chromosome 2q31.
  • Bardet-Biedl syndrome, type 6: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 6 is caused by a defect in chromosome 20p12.
  • Bardet-Biedl syndrome, type 7: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 7 is caused by a defect in chromosome 4q27.
  • Bardet-Biedl syndrome, type 8: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 8 is caused by a defect in chromosome 14q32.11.
  • Bardet-Biedl syndrome, type 9: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 9 is caused by a defect in chromosome 7p14.
  • Bassoe syndrome: A very rare syndrome characterized primarily by hypogonadism, cataracts during infancy and muscle weakness.
  • Benign prostate hypertrophy: Non-cancerous prostrate enlargement common with aging
  • Bent penis: Abnormal bending or curvature of the penis
  • Bentham-Driessen-Hanveld syndrome: A rare syndrome characterized mainly by the association of undescended testes, long thin fingers and mental retardation.
  • Biemond syndrome type 2: A rare inherited condition characterized by mental retardation, obesity, polydactyly and underdeveloped genitals.
  • Bindewald-Ulmer-Muller syndrome: A rare syndrome characterized mainly by a heart defect, and mental and growth retardation.
  • Black widow spider envenomation: The black widow spider bite is toxic to the nerves and can cause serious symptoms. The black widow spider is most commonly found in North America.
  • Bladder cancer: Bladder cancer refers to any of several types of malignant growths of the urinary bladder. It is a disease in which abnormal cells multiply without control in the bladder.
  • Blepharoptosis -- aortic anomaly: A rare disorder characterized mainly by the presence of droopy upper eyelids and an abnormal aorta.
  • Blethen-Wenick-Hawkins syndrome: A rare syndrome characterized mainly by short stature, skeletal abnormalities and reduced pituitary gland functioning.
  • Bloody ejaculation: Blood appearing in the ejaculate after male ejaculation
  • Bloody semen: Blood appearing in ejaculated semen
  • Body symptoms: Symptoms affecting the entire body features.
  • Boggy enlarged prostate: enlarged painful prostate
  • Borjeson Syndrome: A rare genetic disorder characterized by severe mental deficiency, large ears, hypogonadism and other abnormalities.
  • Bosma-Henkin-Christiansen syndrome: A rare syndrome characterized mainly by a reduced sense of smell, an underdeveloped nose and hypogonadism.
  • Boucher-Neuhauser syndrome: A very rare disorder characterized by spinocerebellar ataxia, eye abnormalities and a failure of the pituitary to stimulate gonadal development during puberty.
  • Brachycephalofrontonasal dysplasia: A very rare syndrome characterized primarily by widely spaced eyes and other head and face abnormalities.
  • Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia: A rare syndrome characterized mainly by short digits, extra digits and a small or absent shin bone.
  • Brain -- bone -- fat: A rare inherited disease characterized by bone cysts and progressive presenile dementia.
  • Calcification of basal ganglia with or without hypocalcemia: Calcification of a part of the brain called the basal ganglia. That calcification may be associated with conditions such as hypothyroidism, cytomegalovirus, and AIDS or may occur for no apparent reason. The severity of the condition may vary greatly from asymptomatic to neurological, psychiatric and movement disorders. The disorder may also progress at variable rates or remain stable depending on the underlying disease process.
  • Camera-Marugo-Cohen syndrome: A rare syndrome characterized mainly by mental retardation, muscle weakness, obesity and an asymmetrical body.
  • Carbohydrate deficiency glycoprotein syndrome type II: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 2 is caused by a genetic defect which involves the gene for a particular enzyme (Golgi localized N-acetyl-glucosaminyltransferase II). Type 2 tends to have more severe psychomotor retardation than type 1 but there is no peripheral neuropathy or underdeveloped cerebellum.
  • Cardiocranial syndrome: A rare syndrome characterized mainly by heart and skull abnormalities.
  • Cardiomyopathy -- hypogonadism -- metabolic anomalies: A rare syndrome characterized mainly by heart muscle disease, hypogonadism, blindness, deafness and metabolic anomalies. Puberty was normal despite the hypogonadism.
  • Cardiomyopathy, hypogonadism, collagenoma syndrome: A rare inherited condition characterized primarily by skin nodules. The skin nodules may be associated with organ system involvement resulting in a variety of other symptoms.
  • Cataract -- intellectual deficit -- anal atresia -- urinary defects: A very rare syndrome characterized mainly by cataracts, mental retardation and genitourinary tract abnormalities and absent anal opening.
  • Cataract deafness hypogonadism: A very rare syndrome characterized mainly by deafness, cataracts and a deficiency of sex hormone production.
  • Cathinone poisoning: Cathinone comes from the leaves of the Khat plant which is native to eastern Africa. Cathinone is a stimulant as well as have pain killing, weight loss and neuromuscular effects. The psychoactive effects are usually utilized by chewing on the leaves of the plant but sometimes dried leaves are used.
  • Caudal appendage -- deafness: A very rare syndrome characterized mainly by deafness, finger bone abnormalities and a spinal extension giving a tail-like appearance (caudal appendage).
  • Cephalothoracic progressive lipodystrophy: A rare acquired disorder that involves adipose tissue abnormalities and is characterized by loss of adipose tissue mainly in the trunk and arms.
  • Cerebro-oculo-nasal syndrome: A rare syndrome characterized mainly by eye, nose and brain malformations.
  • Cervical ribs, sprengel anomaly, anal atresia, urethral obstruction: A rare disorder characterized mainly by kidney and urinary system abnormalities, scoliosis and omphalocele. The features of the disorder are variable with male cases tending to be more severe than female cases. Only a few cases of this condition have been reported.
  • Chemical poisoning -- Toluene Diisocyanate: Toluene Diisocyanate is a chemical used mainly in the manufacture of elastomers and polyurethane foams. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Trichloroethylene: Trichloroethylene is a chemical used mainly as an industrial solvent and in adhesives, lacquer, fire retardants and house cleaning solvents. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chlamydia: Common sexually transmitted disease often without symptoms.
  • Chlamydial infection: Infection from Chlamydia genus.
  • Chorditis: Inflammation of a cord, usually the vocal or spermatic cord. The inflammation is most often caused by overuse or abuse of the voice but may also be caused by cancer.
  • Chromosome 1, monosomy 1p34 p32: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as mental retardation, fingernail anomalies and testicular problems.
  • Chromosome 1, trisomy 1q32 qter: A rare chromosomal disorder where duplication of a portion of chromosome 1 causes various abnormalities such as retarded fetal growth, facial anomalies, mental retardation, stillbirth, heart defects and finger and toe abnormalities.
  • Chromosome 10 ring:
  • Chromosome 10 ring syndrome: A rare chromosomal disorder where genetic material from one or both ends of chromosome 10 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing.
  • Chromosome 11, Partial Trisomy 11q: A very rare genetic disorder caused by a duplication of part of chromosome 11q. The characteristic symptoms of the disorder are delayed growth before and after birth, mental retardation (varying severity) and skull and facial defects. The type and severity of symptoms that can occur are variable.
  • Chromosome 11, deletion 11p: A syndrome that is caused by the deletion of short arm (p) of chromosome 11. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted.
  • Chromosome 11q duplication syndrome: A rare chromosomal disorder where there are three copies of the long arm (q) of chromosome 11 rather than the normal two resulting in various abnormalities. The type and severity of symptoms depend on the amount and location of genetic material duplicated.
  • Chromosome 12p deletion: A rare chromosomal disorder where there is a deletion of the short arm (p) of chromosome 12 resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted.
  • Chromosome 12p deletion syndrome: A rare chromosomal disorder where there is a deletion of the short arm (p) of chromosome 12 resulting in various abnormalities.
  • Chromosome 13 ring syndrome: A rare chromosomal disorder where genetic material from one or both ends of chromosome 13 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing.
  • Chromosome 14 trisomy: A rare chromosomal disorder involving duplication of genetic material from chromosome 14 resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
  • Chromosome 14 trisomy syndrome: A rare chromosomal disorder involving duplication of genetic material from chromosome 14 resulting in various abnormalities.
  • Chromosome 14, trisomy mosaic: A rare chromosomal disorder characterized by retarded growth before and after birth, mental retardation, developmental delay and various physical abnormalities. The type and severity of symptoms may vary between patients.
  • Chromosome 15q26-qter Deletion Syndrome: A rare disorder where a portion of genetic material on a particular chromosomal location (15q26-qter) is missing which manifests in a variable range of symptoms.
  • Chromosome 18 deletion syndrome: A rare chromosomal disorder where a portion of chromosome 18 is missing.
  • Chromosome 18, Tetrasomy 18p: A rare chromosomal disorder where there are four copies of short arm of chromosome 18 instead of the normal two which results in various genital, kidney, digital, head and face abnormalities.
  • Chromosome 18q, partial deletion: A rare chromosomal disorder involving deletion of genetic material from the long arm of chromosome 18. The type and severity of symptoms are determined by the amount and location of the lost genetic material.
  • Chromosome 18q- Syndrome: A rare chromosomal disorder where a portion of chromosome 18 is missing. The type and severity of symptoms is determined by the amount of genetic material that is missing.
  • Chromosome 2, trisomy 2p: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 2 is duplicated so there is three copies of it rather than the normal two.
  • Chromosome 2, trisomy 2q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 2 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Chromosome 21, tetrasomy 21q: A rare chromosomal disorder where there is four copies of the long arm of chromosome 21 instead of the normal two which results in various physical and mental anomalies.
  • Chromosome 22, trisomy: A very rare disorder where there is an extra copy of chromosome 22 in all the body cells. The condition is usually fatal soon after birth or during the fetal stage.
  • Chromosome 2p duplication syndrome: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 2 is duplicated so there is three copies of it rather than the normal two.
  • Chromosome 2p16.1-p15 Deletion Syndrome: A rare genetic disorder characterized by a range of manifestations including mental retardation and skull and facial anomalies.
  • Chromosome 2q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 2 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Chromosome 3, monosomy 3p25: A rare chromosomal disorder characterized by mental retardation, short stature, deafness, extra digits, facial anomalies and various other abnormalities.
  • Chromosome 3, monosomy 3q13: A rare chromosomal disorder characterized by a range of abnormalities including facial anomalies, kidney dysfunction, large head, small penis and impaired joint mobility.
  • Chromosome 3, trisomy 3p: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 3 is duplicated so there is three copies of it rather than the normal two.
  • Chromosome 3, trisomy 3q: A rare chromosomal disorder where a portion of the long arm (q) of chromosome 3 is duplicated so there is three copies of it rather than the normal two. The condition is characterized by mental and growth deficiency, broad nose root and excessive hair growth.
  • Chromosome 4, trisomy 4p: A rare chromosomal disorder where a portion of chromosome four is duplicated so there is three copies of it instead of the normal two.
  • Chromosome 6 Ring: A rare chromosomal disorder where the ends of chromosome 6 have been deleted and the two broken ends have rejoined to form a ring shape resulting in a range of symptoms determined by the size of the genetic deletion.
  • Chromosome 6 ring syndrome: A rare chromosomal disorder where the ends of chromosome 6 have been deleted and the two broken ends have rejoined to form a ring shape resulting in a range of symptoms determined by the size of the genetic deletion.
  • Chromosome 6, monosomy 6q: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Chromosome 6q deletion syndrome: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Chromosome 6q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 6 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Chromosome 7 ring syndrome: A rare chromosomal disorder where the ends of chromosome 7 have been deleted and the two broken ends have rejoined to form a ring shape resulting in a range of symptoms determined by the size of the genetic deletion.
  • Chromosome 7, monosomy 7q3: A very rare chromosomal disorder involving a deletion of material from chromosome 7 at a location known as q3 which results in a wide range of abnormalities.
  • Chromosome 7, trisomy 7p: A rare chromosomal disorder where there are three copies of all or part of the short arm (p) of chromosome 7 rather than the normal two. The type and severity of symptoms is determined by the location and size of the genetic material duplicated.
  • Chromosome 7, trisomy 7q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Chromosome 7p duplication syndrome: A rare chromosomal disorder where there are three copies of all or part of the short arm (p) of chromosome 7 rather than the normal two. The type and severity of symptoms is determined by the location and size of the genetic material duplicated.
  • Chromosome 7q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Chromosome 8 recombinant syndrome: A rare recombinant chromosomal disorder involving chromosome 8 which results in various abnormalities.
  • Chromosome 8, trisomy 8p: A rare chromosomal disorder where the short arm (p) of chromosome 8 is duplicated resulting in three copies instead of two. The type and severity of symptoms depends on the location and length of genetic material duplicated.
  • Chromosome 8, trisomy 8q: A rare chromosomal disorder where the long arm (q) of chromosome 8 is duplicated resulting in variable abnormalities depending on the location and length of genetic material deleted.
  • Chromosome 8p duplication syndrome: A rare chromosomal disorder where the short arm (p) of chromosome 8 is duplicated resulting in three copies instead of two. The type and severity of symptoms depends on the location and length of genetic material duplicated.
  • Chromosome 8q duplication syndrome: A rare chromosomal disorder where the long arm (q) of chromosome 8 is duplicated resulting in variable abnormalities depending on the location and length of genetic material deleted.
  • Chromosome 9 trisomy syndrome: A rare chromosomal disorder where there are three copies of chromosome 9 in the body's cells instead of the normal two resulting in various abnormalities.
  • Chromosome 9, Partial Monosomy 9p: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 9 is missing resulting in various abnormalities. The type and severity of symptoms is determined by the amount of genetic material that is missing.
  • Chromosome 9, monosomy 9p: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 9 is missing resulting in various abnormalities.
  • Chromosome 9, trisomy: A rare chromosomal disorder where there are three copies of chromosome 9 in the body's cells instead of the normal two resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
  • Chromosome 9/mosaic: A rare chromosomal disorder where chromosome 9 is duplicated in some of the body's cells resulting in various abnormalities determined by the type and number of cells that contain the extra genetic material.
  • Chromosome 9q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 9 resulting in various abnormalities.
  • Chromosome diploid-triploid mosaicism syndrome: A rare chromosomal disorder involving chromosomal duplication, triplication and mosaicism.
  • Chronic Kidney Disease: Long-term and generally irreversible disease of the kidneys due to infection, obstruction, congenital diseases or generalised diseases causing failure of the kidneys' normal functions.
  • Chronic herpes-like penile ulcers: formation of vesicles similar to the presentation in herpes
  • Chronic interstitial cystitis:
  • Chronic prostate blockage like symptoms: conditions which cause chronic symptoms similar to that when there is a blockage to prostate secretions
  • Chronic prostate pain symptoms: conditions which cause chronic pain similar to that of pain due to a prostatic pathology
  • Chronic prostate symptoms: symptoms related to the prostate includes painful micturition, hestiatancy and frequency of micturition
  • Chronic prostate-related urinary dribbling: weak urinary stream
  • Chronic prostate-related urinary symptoms: Symptomsinclude urinary frequency, urgency, urgency incontinence, voiding at night (nocturia), weak urinary stream, hesitency (needing to wait for the stream to begin), intermittency (when the stream starts and stops intermittently), straining to void, dysuria (burning sensation in the urethra), and dribbling
  • Chronic prostate-related weak urinary stream: weak urinary stream
  • Chudley syndrome 1: A rare syndrome characterized by mental retardation, obesity, hypogonadism and a distinctive mouth.
  • Clark-Baraitser syndrome: A very rare syndrome characterized mainly by tallness, large head, mental retardation and various facial anomalies.
  • Cleft palate -- cardiac defect -- genital anomalies -- ectrodactyly: A very rare syndrome characterized by variable symptoms including cleft palate, heart defects, genital anomalies and hand and foot malformations.
  • Condoms and diaphragms induced allergies: Condoms and diaphragms induced allergies are an adverse reaction by the body's immune system to the latex in condoms and diaphragms.
  • Congenital adrenal hyperplasia: A condition where excessive secretion of adrenocortical androgens cause a somatic masculization or ?virilization? effect on a fetus or baby. Symptoms in girls may include masculization of sex organs, low voice, acne, amenorrhea and masculine hair distribution and muscle growth. Symptoms in boys include enlarged penis, small testes. Children with the condition are usually taller than average but develop into short adults. Also called adrenogenital syndrome or adrenal virilism.
  • Congenital adrenal hyperplasia -- simple virilizing form in females: A group of disorder that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The simple virilizing form involves a moderate deficiency of 21-hydroxylase and differs in its effects on males and females.
  • Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency: A rare genetic condition involving deficiency of 17-alpha-hydroxylase which impairs androgen production by the testes and estrogen production by the ovaries. This results in lack of development of secondary sexual characteristics and hypertension as well as other anomalies.
  • Congenital giant megaureter: A rare condition where the patient is born with an abnormally dilated ureter. The anomaly is often associated with other defects or anomalies. The severity of the anomaly is variable.
  • Congenital penile anomalies: Congenital penile anomalies are birth defects of the penis.
  • Constant scrotal pain: Constant scrotal pain is discomfort is the scrotum that is steady and continual.
  • Constant testicular pain: Constant testicular pain is steady and continual discomfort in the testicles.
  • Craniofrontonasal Syndrome: A congenital condition with multiple anomalies associated with mental retardation and skeletal disfigurement.
  • Craniofrontonasal dysplasia: A rare genetic disorder mainly found in females and characterized by premature closing of skull bones and craniofacial and limb abnormalities.
  • Craniofrontonasal syndrome Teebi type: A very rare syndrome characterized primarily by widely spaced eyes and other head and face abnormalities.
  • Craniostenosis with congenital heart disease mental retardation: A very rare disorder characterized mainly by premature fusion of the sagittal skull bones, mental retardation and heart disease that is present at birth. The disorder generally involves other variable features.
  • Craniosynostosis -- congenital heart disease -- mental retardation: A rare syndrome characterized mainly by heart and skull abnormalities as well as mental retardation.
  • Cryptorchidism: A condition where one or both testes fail to descend to the normal position in the scrotum. Also called cryptorchis or undescended testis.
  • Cryptorchidism in children: Cryptorchidism in children refers to a boy who has an undescended testicle.
  • Culler-Jones syndrome: A very rare syndrome characterized mainly by hypopituitarism (low pituitary hormone level) which affects other hormone levels and an extra little finger.
  • Cystic Fibrosis: Cystic fibrosis is a hereditary disease affecting the exocrine (mucus) glands of the lungs, liver, pancreas, and intestines, causing progressive disability due to multisystem failure.
  • Cystic fibrosis -- gastritis -- megaloblastic anaemia: A rare syndrome characterized mainly by cystic fibrosis, metaloblastic anemia, mental retardation and gastritis due to helicobacter pylori.
  • De Grouchy Syndrome: A rare chromosomal disorder where a portion of chromosome 18 is missing. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted.
  • De la Chapelle syndrome: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
  • Deafness -- pili torti -hypogonadism: An inherited condition characterized by twisted hairs, hypogonadism and nerve deafness.
  • Deafness hypogonadism syndrome: A rare condition characterized by the combination of hypogonadism and deafness.
  • Deafness-mental retardation, Martin-Probst type: A rare disorder characterized mainly by deafness and mental retardation.
  • Decreased penile sensation: Decreased penile sensation is a lowered level of feeling in the penis.
  • Del (2) (q37.1-qter) and dup (14) (q31.2-qter): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in two reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Del Castillo's syndrome: Infertility due to absence of germinal cells which are needed to make sperm.
  • Del(1) (q25-q32): A very rare chromosomal disorder where a portion of the long arm (q25-q32) of chromosome one is missing. The range and severity of symptoms is variable.
  • Del(1) (q42-qter): A very rare chromosomal disorder where a portion of the long arm (q42-qter) of chromosome one is missing. The type and severity of symptoms is variable.
  • Delayed ejaculation: A condition which is characterized by a delay in the males ability to ejaculate
  • Deletion 10q: A rare disorder caused by the deletion of a portion of chromosome 10q. The range and severity of symptoms is determined by the size of the portion that is deleted.
  • Deletion 11p: A syndrome that is caused by the deletion of short arm (p) of chromosome 11. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted.
  • Deletion 18q: A rare chromosomal disorder where a portion of chromosome 18 is missing. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted.
  • Deletion 6q: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 1: Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk of developing Type 2 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 1 is linked to a defect on chromosome 2q37.3.
  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 2: Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk of developing Type 2 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 2 is linked to a defect on chromosome 12q24.2.
  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 3: Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk of developing Type 2 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 3 is linked to a defect on chromosome 20q12-q13.1.
  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 4: Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk of developing Type 2 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 4 is linked to a defect on chromosome 5q34-q35.2.
  • Diabetes-like symptoms: Symptoms similar to those of diabetes
  • Diabetic neuropathy: nerve damage which maybe motor, sensory and autonomic
  • Diphallus -- rachischisis -- imperforate anus: A very rare syndrome characterized mainly by genital abnormalities, absent anal opening and malformed vertebrae.
  • Discharge from penis: abnormal discharge from the penis which is not urine or semen
  • Distal Trisomy 11q: A very rare genetic disorder caused by a duplication of part of chromosome 11q. The characteristic symptoms of the disorder are delayed growth before and after birth, mental retardation (varying severity) and skull and facial defects. The type and severity of symptoms that can occur are variable.
  • Dup (2) (p21-p13): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (2) (pter-p23): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in the few reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (2) (q11.2-q13): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (3) (p22-p14): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in two reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (3) (pter-p25): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in nine reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup(1) (p35-p31): A very rare chromosomal disorder where a portion of the short arm (p35-p31) of chromosome one is duplicated. The reported case resulted in death at 6 weeks of age.
  • Duplication 2p: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 2 is duplicated so there is three copies of it rather than the normal two.
  • Duplication 2q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 2 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Duplication 7p: A rare chromosomal disorder where there are three copies of all or part of the short arm (p) of chromosome 7 rather than the normal two. The type and severity of symptoms is determined by the location and size of the genetic material duplicated.
  • Duplication 7q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Duplication 8p: A rare chromosomal disorder where the short arm (p) of chromosome 8 is duplicated resulting in three copies instead of two. The type and severity of symptoms depends on the location and length of genetic material duplicated.
  • Duplication 8q: A rare chromosomal disorder where the long arm (q) of chromosome 8 is duplicated resulting in variable abnormalities depending on the location and length of genetic material deleted.
  • Dyskeratosis congenita of Zinsser-Cole-Engman: An inherited condition characterized by recurring painful mouth ulcers, skin pigmentation and nail abnormalities.
  • Dysostosis acral with facial and genital abnormalities: A very rare inherited disorder characterized by short stature and head, face, skeletal and genital abnormalities. The facial appearance is that of a two-month old fetus. The severity and range of symptoms is variable. This dominantly inherited form of Robinow syndrome tends to be milder than the recessive form.
  • Dystrophia myotonica 1: A rare genetic disorder characterized by myotonia, muscle atrophy, cataracts and hypogonadism.
  • EEC syndrome: A rare genetic disorder characterized by absence of fingers and toes, ectodermal dysplasia and cleft lip or cleft palate.
  • Ectodermal dysplasia -- mental retardation -- CNS malformation: A rare syndrome characterized mainly by mental retardation, central nervous system disorders and skin, hair and nail abnormalities.
  • Ectodermal dysplasia -- mental retardation -- central nervous system malformation: A rare syndrome characterized by severe mental retardation, hypothyroidism, abnormal brain development and hair, teeth and nail abnormalities.
  • Ectodermal dysplasia, Berlin type: A rare syndrome characterized mainly by the absence of many or all teeth, a lack of hair, mental retardation and skin abnormalities.
  • Ectrodactyly -- Ectodermal Dysplasia -- Cleft Lip/Palate Syndrome, Type 1: EEC (Ectrodactyly, ectodermal dysplasia, cleft lip/palate) is a rare inherited condition characterized by split hand and foot deformities of variable severity, cleft lip or palate and teeth and hair anomalies. There are two main types of EEC which differ in the origin of the genetic defect. Type 1 is caused by a defect on chromosome 7q11. The severity and type of symptoms and deformities is highly variable.
  • Ectrodactyly -- Ectodermal Dysplasia -- Cleft Lip/Palate Syndrome, Type 3: EEC (Ectrodactyly, ectodermal dysplasia, cleft lip/palate) is a rare inherited condition characterized by split hand and foot deformities of variable severity, cleft lip or palate and teeth and hair anomalies. There are two main types of EEC which differ in the origin of the genetic defect. Type 3 is caused by a defect on chromosome 3q27. The severity and type of symptoms and deformities is highly variable.
  • Ejaculate blood: blood in the semen, called hematospermia, maybe undectable( microscopic) or visible in the ejaculation fluid
  • Ejaculation symptoms: Symptoms related to ejaculation and orgasm
  • Emanuel syndrome: A rare chromosomal disorder where a portion of chromosome 11 is translocated with a portion of chromosome 22. The disorder involves a wide range of abnormalities such as kidney, genital and heart abnormalities, mental retardation, small head and failure to thrive.
  • Endocrine-Cerebroosteodysplasia: A rare condition observed in six members from two families. The condition is severe with all affected individuals dying before, during or soon after birth. A number of the pregnancies were voluntarily terminated due to the detected malformations. Endocrine-Cerebroosteodysplasia primarily involves brain, skeletal and endocrine abnormalities.
  • Endodermal sinus tumor: A form of malignant germ cell tumor that occurs mainly in young children. They can occur in the testis, ovaries, uterus, abdomen, thorax, tailbone region, vagina, liver, retroperitoneum and pineal ventricle of the brain. Symptoms will vary depending on the exact location of the tumor.
  • Endomyocardial fibroelastosis: A rare heart malformation involving an abnormal thickening of the part of the heart muscle called the endocardium which affects the heart's function. Death is common in infancy and during early childhood.
  • Enlarged testicle: Enlargement of the male testicle to a size considered to be more than normal
  • Epididymal nodules: presence of nodules in the epididymis
  • Epididymitis: Infection of the epididymis (testicle tube)
  • Epididymo-orchitis: A condition which is characterized by inflammation of the epididimis and testes of a male
  • Erectile disorder:
  • Erectile dysfunction: The inability to obtain on normal erection
  • Erection problems:
  • Eunuchoidism familial: A rare inherited defect that affects production of gonadotropin which affects puberty and the development of secondary sexual characteristics.
  • Face symptoms: Symptoms affecting the face
  • Facial dysmorphism -- shawl scrotum -- joint laxity syndrome: A very rare syndrome characterized mainly by loose joints, facial anomalies and a shawl scrotum.
  • Faciodigitogenital syndrome, recessive form: A rare syndrome characterized by facial, digital and genital abnormalities.
  • Familial renal cell carcinoma: A genetic form of kidney cancer that develops in the lining of the tubules in the kidney and tends to run in families.
  • Fanconi pancytopenia: A rare genetic disorder characterized by upper limb defects and kidney abnormalities.
  • Femoral facial syndrome: A rare genetic disorder characterized by underdeveloped femur, short nose and cleft palate.
  • Fluoxetine -- Teratogenic Agent: There is evidence to indicate that exposure to Fluoxetine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Fontaine-Farriaux-Blanckaert syndrome: A rare syndrome characterized by premature fusion of skull bones as well as various other abnormalities.
  • Forbes-Albright syndrome: A rare condition where a hormone secreting pituitary or hypothalamic tumor causes galactorrhea and amenorrhea.
  • Foreskin conditions: Conditions that affect the male foreskin
  • Foreskin itch: An sensation to scratch the foreskin
  • Foreskin paresthesia/ tingling: A loss of sensation located at or around the foreskin
  • Foreskin rash: An eruption on the skin of the foreskin
  • Foreskin symptoms: Symptoms affecting the foreskin of the penis
  • Foreskin tingling/ paresthesia: A tingling sensation located on the foreskin
  • Fragile-X Syndrome: A rare inherited characterized by various physical anomalies as well as mental retardation. The symptoms are milder in females.
  • Froelich's syndrome: A rare condition where an endocrine abnormality (caused by such things as a pituitary tumor or damage to the hypothalamus) affects hormone levels which results in a variety of symptoms.
  • GAPO syndrome: A rare condition characterized by retarded growth, alopecia, otpic atrophy and failure of teeth to erupt.
  • Garret-Tripp syndrome: A rare syndrome characterized mainly by extra digits, a lack of hair and scaly skin on the scalp, face and neck.
  • Genital anomaly -- cardiomyopathy: A rare syndrome characterized by the association of heart disease with genital abnormalities.
  • Genital herpes: Sexually transmitted infection of the genital region.
  • Genital lesions in male: most commonly are ulcers which are situated in the genital area
  • Genital lesions in the male: Genital lesions in the male refer to ulcers or sores that develop on the genitals.
  • Genital symptoms: Symptoms affecting the sex organs.
  • Genital warts: Skin warts in the genital regions.
  • Gigantism: Gigantism refers to abnormally high linear growth due to excessive action of insulin-like growth factor-I (IGF-I) while the epiphyseal growth plates are open during childhood.
  • Gonadotropin-independent precocious puberty: A rare disorder affecting males where premature puberty is not caused by a premature release of gonadotropin hormones.
  • Gonorrhea: Common sexually transmitted disease often without symptoms.
  • Gradual onset of scrotal swelling: Gradual onset of scrotal swelling is a slow development of puffiness or abnormal enlargement of the scrotum.
  • Granuloma inguinale: Granulomous disease spread sexually.
  • Growth Hormone Deficiency: A deficiency in growth hormone which results in poor growth.
  • Growth Hormone Receptor Deficiency: Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from binding and being used. Hence there are high levels of free growth hormone in the plasma. Type II involves a problem with the processing of the growth hormone once it has been bound properly to the cell surface.
  • Head symptoms: Symptoms affecting the head or brain
  • Hematochromatosis: Hemochromatosis is the abnormal accumulation of iron in parenchymal organs, leading to organ toxicity. It is the most common inherited liver disease in whites and the most common autosomal recessive genetic disorder.
  • Hemochromatosis: Excess of iron leading to problems with joints, liver, heart and pancreas.
  • Hemochromatosis-related diabetes: A single-gene disease that causes iron accumulation in the tissues of the body. Diabetes is a primary complication if hemochromatosis goes untreated. Hemochromatosis is sometimes referred to as "bronze diabetes."
  • Hemolytic anaemia, lethal -- genital anomalies: A very rare syndrome characterized mainly by genital abnormalities and hemolytic anemia which often causes death.
  • Hemolytic anemia, lethal -- genital anomalies: A very rare syndrome characterized mainly by genital abnormalities and hemolytic anemia which often causes death.
  • Hemospermia: The presence of blood in the semen.
  • Herpes-like penile ulcers: formation of vesicles similar to the presentation in herpes
  • Holoprosencephaly deletion 2p: A very rare syndrome characterized mainly by the failure of the brain to separate into two lobes, facial deformities and various other anomalies.
  • Holoprosencephaly, recurrent infections, and monocytosis: A rare syndrome characterized by recurring infections and a brain anomaly. Death usually occurs during the first years of life due to sepsis.
  • Human Papillomavirus: Very common sexually transmitted disease causing genital warts and associated with certain cancers.
  • Hunter-Carpenter-Macdonald syndrome: A very rare syndrome characterized by various abnormalities including small head, facial anomalies, mental retardation and hair, skin and nail anomalies. Fetal exposure to alcohol is believed to be a factor in the syndrome.
  • Hydrocele: Swollen testes due to fluid
  • Hydrocephalus obesity hypogonadism: A very rare syndrome characterized mainly by obesity, buildup of fluid inside the skull (hydrocephalus) and impaired sex hormone production.
  • Hyperpigmentation, Cutaneous, With Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, Hearing Loss, And Hypogonadism: A rare syndrome characterized by various skin and nail anomalies as well as other problems.
  • Hyperprolactinemia: High levels of prolactin in the blood.
  • Hypersecretion of growth hormone: increased production of growth hormone from the pituitary gland
  • Hypogonadism -- mitral valve prolapse -- mental retardation: A very rare syndrome characterized mainly by a heart disorder, hypogonadism and mental retardation.
  • Hypogonadism hypogonadotropic due to mutations in GR hormone: Hypogonadism hypogonadotropic due to mutations in GR hormone is a condition where defects in the gene for gonadotropin-releasing hormone results in problems with sexual maturation during development. The symptoms may vary in severity depending on the degree of mutation.
  • Hypogonadism, isolated, hypogonadotropic: A rare condition involving a deficiency of sex hormones (leutinizing and follicle-stimulating hormone) which results in partial or complete failure of puberty.
  • Hypogonadism, primary -- partial alopecia: A very rare syndrome characterized mainly by hypogonadism and the presence of hair in the middle of the scalp only.
  • Hypogonadotropic hypogonadism alopecia: A very rare syndrome characterized by partial alopecia and lack of secondary sex hormone production.
  • Hypogonadotropic hypogonadism without anosmia, X-linked: A rare X-linked disorder involving a deficiency of sex hormones (leutinizing and follicle-stimulating hormone). It is similar to Kallman syndrome but the sense of smell is preserved.
  • Hypopituitarism: A condition characterized by diminished hormonal section by the pituitary gland
  • Hypopituitarism -- micropenis -- cleft lip palate: A very rare syndrome characterized mainly by low pituitary hormone level, small penis and a cleft lip and palate.
  • Hypopituitarism postaxial polydactyly: A very rare syndrome characterized mainly by hypopituitarism (low pituitary hormone level) which affects other hormone levels and an extra little finger.
  • Hypospadias: Congenital defect with misplaced urinary opening
  • IMAGe syndrome: A rare syndrome characterized by retarded fetal growth, abnormal bone development, underdeveloped adrenal glands and genital abnormalities.
  • Ichthyosis and male hypogonadism: A very rare syndrome characterized mainly by scaly skin and insufficient hormone production by the male gonads.
  • Ichthyosis male hypogonadism: A very rare syndrome characterized mainly by scaly skin and insufficient hormone production by the male gonads.
  • Impossible syndrome: A very rare syndrome (only one reported case) characterized a range of severe malformations, premature birth and stillbirth.
  • Impotence: Difficulty starting or maintaining an erection
  • Impotence (Erectile dysfunction):
  • Induration of the prostate: swelling of the prostate gland
  • Inhibited ejaculation: The inhibition of a males ability to ejaculate
  • Intercourse symptoms: Symptoms related to the act of sexual intercourse.
  • Intermittent herpes-like penile ulcers: formation of vesicles similar to the presentation in herpes
  • Intermittent prostate blockage like symptoms: conditions which cause symptoms similar to that when there is a blockage to prostate secretions
  • Intermittent prostate pain symptoms: conditions which cause intermittent pain similar to that of pain due to a prostatic pathology
  • Intermittent prostate symptoms: symptoms related to the prostate includes painful micturition, hestiatancy and frequency of micturition
  • Intermittent prostate-related urinary dribbling: weak urinary stream
  • Intermittent prostate-related urinary symptoms: Symptomsinclude urinary frequency, urgency, urgency incontinence, voiding at night (nocturia), weak urinary stream, hesitency (needing to wait for the stream to begin), intermittency (when the stream starts and stops intermittently), straining to void, dysuria (burning sensation in the urethra), and dribbling
  • Intermittent prostate-related weak urinary stream: weak urinary stream
  • Intrauterine growth retardation -- metaphyseal dysplasia -- adrenal hypoplasia congenita -- genital anomalies: A rare syndrome characterized by retarded fetal growth, abnormal bone development, underdeveloped adrenal glands and genital abnormalities.
  • Irons-Bhan syndrome: A very rare syndrome characterized mainly by lymphoedema in the legs, heart defects and a hydrocele (swollen testicles).
  • Irritation of scrotum skin: A condition which is characterized by irritation of the skin of the scrotum
  • Johanson-Blizzard Syndrome: A rare genetic disorder involving a range of abnormalities including a characteristic beak-like small nose, hypothyroidism and deafness.
  • Kallmann Syndrome: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance.
  • Kallmann Syndrome 5: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. The symptoms and their severity may be somewhat variable. Type 5 is linked to a defect on chromosome 8q12.1.
  • Kallmann Syndrome 6: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. The symptoms and their severity may be somewhat variable. Type 6 is linked to a defect on chromosome 10q24.
  • Kallmann syndrome 2: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 2 is caused by a genetic defect located at chromosome 8p11.2-p11.1.
  • Kallmann syndrome, type 1, X-linked: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 1 is caused by a genetic defect located at chromosome Xp22.3.
  • Kallmann syndrome, type 3, recessive: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 3 is recessively inherited and the genetic defect is located at chromosome 20p13.
  • Kallmann syndrome, type 4: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 4 is caused by a genetic defect located at chromosome 3p21.1.
  • Kidney symptoms: Symptoms affecting one or both kidneys.
  • Klinefelter syndrome: A genetic condition where males have at least one extra X chromosome or extra copies of both the X and Y chromosomes in each cell. Normally male cells contain one X and one Y chromosome in each cell. The condition is not inherited but is a result of problems during cell division. Klinefelter syndrome variants is a more severe form of the condition as it involves more than one extra X or X and Y chromosome in each cell.
  • Klinefelter syndrome variant:
  • Klinefelter syndrome, variants: A genetic condition where males have at least one extra X chromosome or extra copies of both the X and Y chromosomes in each cell. Normally male cells contain one X and one Y chromosome in each cell. The condition is not inherited but is a result of problems during cell division.
  • Lactotroph adenoma: A benign pituitary tumor that secretes excessive prolactin which can affect the functioning of the reproductive system - testes and ovaries. The tumor may also grow large enough to compress adjacent structures such as the eye nerves.
  • Lambert-Eaton Myasthenic Syndrome: A condition where a patient with a carcinoma suffers from progressive muscular weakness.
  • Laron Dwarfism: Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from binding and being used. Hence there are high levels of free growth hormone in the plasma. Type II involves a problem with the processing of the growth hormone once it has been bound properly to the cell surface.
  • Laron Pituitary Dwarfism: Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from binding and being used. Hence there are high levels of free growth hormone in the plasma. Type II involves a problem with the processing of the growth hormone once it has been bound properly to the cell surface.
  • Laron Syndrome: Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from binding and being used. Hence there are high levels of free growth hormone in the plasma. Type II involves a problem with the processing of the growth hormone once it has been bound properly to the cell surface.
  • Laron Type Pituitary Dwarfism 1: Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from binding and being used. Hence there are high levels of free growth hormone in the plasma. Type II involves a problem with the processing of the growth hormone once it has been bound properly to the cell surface.
  • Laron-type Dwarfism Phenotypic Syndrome: Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from binding and being used. Hence there are high levels of free growth hormone in the plasma. Type II involves a problem with the processing of the growth hormone once it has been bound properly to the cell surface.
  • Laurence-Moon Syndrome: A rare inherited disorder characterized by vision loss, impaired hormone production, mental retardation and spastic paraplegia.
  • Leriche syndrome: A rare syndrome caused by a blockage in the terminal aorta which supplies blood to the lower part of the body.
  • Leriche's Syndrome: A condition caused by blockage of the abdominal aorta and iliac artery resulting in wasting of buttock muscles, lack of pulse in femoral arteries and inability to maintain a penile erection.
  • Leukemia: Cancer of the blood cells, usually white blood cells.
  • Leydig cells hypoplasia: A condition resulting from reduced or absent functioning of Leydig cells which leads to insufficient production of the male hormone androgen which can cause problems with sex differentiation in males at puberty. The severity of symptoms varies depending on the degree of functioning of the Leydig cells. Type 1 is a more severe form of the condition where males develop a female appearance whereas type II results in symptoms such as small penis and hypogonadism though the patients has an overall male appearance.
  • Leydig cells hypoplasia, type I: A condition resulting from reduced or absent functioning of Leydig cells which leads to insufficient production of the male hormone androgen which can cause problems with sex differentiation in males at puberty. The severity of symptoms varies depending on the degree of functioning of the Leydig cells. Type 1 is a more severe form of the condition where males develop a female appearance whereas type II results in symptoms such as small penis and hypogonadism though the patients has an overall male appearance.
  • Leydig cells hypoplasia, type II: A condition resulting from reduced or absent functioning of Leydig cells which leads to insufficient production of the male hormone androgen which can cause problems with sex differentiation in males at puberty. The severity of symptoms varies depending on the degree of functioning of the Leydig cells. Type 1 is a more severe form of the condition where males develop a female appearance whereas type II results in symptoms such as small penis and hypogonadism though the patients has an overall male appearance.
  • Lichen planus: Skin rash
  • Lichen sclerosis: Disease causing leathery or dry skin in genital areas.
  • Lissencephaly, X linked -- agenesis of the corpus callosum -- genital anomalies: A rare brain malformation where the surface of the brain is smoother than normal. Absent corpus callosum and genital anomalies are also associated. The severity of the disorder is variable.
  • Lissencephaly, X-linked 2: A rare brain malformation where the surface of the brain is smoother than normal. Genital anomalies are also associated. The severity of the disorder is variable.
  • Lissencephaly, X-linked, 1: Abnormal brain development resulting in an abnormally smooth brain surface which results in neurological symptoms such as mental retardation. This particular type is inherited in a X-linked manner is caused by a defect in the doublecortin gene on chromosome Xq22.3-q23.
  • Lissencephaly, type 1, X-linked: Abnormal brain development characterized by an abnormally smooth brain. This form of the disorder is inherited in a X-linked manner (defect on the DCX gene) and the corpus callosum fails to develop. Males tend to be affected more severely than females.
  • Lump in the testicle: not all lumps in the testicles are tumours and not all tumopurs are malignant, but all lumps must be checked by a physician
  • Lundberg II syndrome: A rare syndrome involving cataracts, reduced hormone production by ovaries or testes and myopathy which mainly involves the facial and muscles close to the trunk.
  • Lymphatic Filariasis: Parasitic worm infection of the lympatic system
  • Lymphocytic choriomeningitis: Rodent-borne viral disease often causing meningitis or encephalitis
  • Lymphogranuloma venereum: Type of chlamydia (sexually transmitted disease)
  • MORM syndrome: A rare syndrome characterized by mental retardation, truncal obesity, small penis and an eye disorder.
  • MacDermot-Winter syndrome: A very rare syndrome characterized mainly by a small head, underdeveloped genitalia and a protrusion of the area between the eyes (glabella).
  • Macrocytosis: Blood condition where average red blood cell size is increased
  • Male Menopause: The gradual changes in hormone status of an ageing male relating to genital and body appearance and sexual function that has been likened to the female menopause.
  • Male conditions: Any conditions that specifically affect the male sex
  • Male genital conditions: Any condition that affects the male genitalia
  • Male genital symptoms: Symptoms affecting the male genitals.
  • Male reproductive symptoms: Symptoms affecting the male reproductive organs.
  • Male sexual conditions: Any condition that affects the ability of a male to have sexual relations
  • Malpuech facial clefting syndrome: A very rare syndrome characterized by mental and physical retardation, wide set eyes, genital abnormalities and a characteristic facial cleft.
  • Marburg virus: Serious virus related to Ebola.
  • Martsolf syndrome: A rare inherited condition characterized by mental retardation, cataracts, small head and hypogonadism (reduced production of hormones by ovaries or testes).
  • McCune-Albright Syndrome: A rare genetic multisystem disorder characterized by abnormal skin pigmentation and endocrine gland dysfunction and replacement of parts of bone tissue with fibrous material.
  • Mens health symptoms: Symptoms closely related to men's health.
  • Mental retardation -- hypotonic facies syndrome, X-linked, 1: A group of rare syndromes characterized by severe mental retardation, unusual facial appearance and other variable abnormalities.
  • Mental retardation -- myopathy -- short stature -- endocrine defect: A very rare syndrome characterized mainly by mental retardation, muscle disease, short stature and endocrine defects.
  • Mental retardation -- short stature -- deafness -- genital: A very rare syndrome characterized mainly by mental retardation, short stature, deafness and genital abnormalities.
  • Mental retardation -- unusual facies -- talipes -- hand anomalies: A very rare syndrome characterized mainly by mental retardation, unusual facial appearance, clubfoot and hand abnormalities.
  • Mental retardation X-linked -- psychosis -- macroorchidism: A rare syndrome characterized by mental retardation, psychosis and abnormally lartge testes. The syndrome is inherited in a X-linked manner.
  • Mental retardation psychosis macroorchidism: A very rare syndrome characterized by mental retardation, psychosis and enlarged testes.
  • Mental retardation, X-linked -- acromegaly -- hyperactivity: A rare syndrome characterized mainly by mental retardation, hyperactivity and enlarged hands, feet and testes.
  • Mental retardation, X-linked -- gynecomastia -- obesity: A rare disorder characterized by mental retardation, obesity, enlarged male breasts, speech problems and other anomalies. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms.
  • Mental retardation, X-linked, Cabezas type: A rare X-linked disorder characterized by mental retardation, muscle wasting, short stature and other problems. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms.
  • Mental retardation, X-linked, Vitale type: A rare disorder characterized by mental retardation and facial and skeletal anomalies. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms. The genetic defect occurs on chromosome Xq24.
  • Mental retardation, X-linked, syndromic, due to JARID1C mutation: A rare disorder characterized by mental retardation, spasticity and other variable features. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms. The disorder is caused by a defect on the JARID1C gene on chromosome Xp11.22-p11.21.
  • Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance: A very rare syndrome characterized by moderate to severe mental retardation, unusual facial appearance and an underdeveloped brain.
  • Mesodermal defects lower type: A very rare syndrome characterized mainly by defects of the lower trunk area such as the pelvic organs.
  • Microcephaly -- hypergonadotropic hypogonadism -- short stature: A very rare syndrome characterized mainly by a small head, short stature and hypogonadism.
  • Microcephaly -- microphthalmos -- blindness: A very rare syndrome characterized mainly by a small head, small eyes and blindness.
  • Microcephaly -- seizures -- mental retardation -- heart disorders: A very rare syndrome characterized mainly by a small head, seizures, mental retardation and heart disorders.
  • Microcephaly micropenis convulsions: A syndrome which is characterized by the association of symptoms such as abnormal facial appearance, short stature and psychomotor retardation.
  • Microphthalmia syndromic, type 6: A rare inherited syndrome characterized mainly by small eyes, malformed ears, small jaw and finger and genital abnormalities. The symptoms are variable to some degree.
  • Mild prostate blockage like symptoms: conditions which cause mild symptoms similar to that when there is a blockage to prostate secretions
  • Mild prostate pain symptoms: conditions which cause mild pain similar to that of pain due to a prostatic pathology
  • Mild prostate symptoms: mild symptoms related to the prostate includes slight pain on micturition, hestiatancy and frequency of micturition
  • Mild prostate-related urinary dribbling: weak urinary stream
  • Mild prostate-related urinary symptoms: Symptomsinclude urinary frequency, urgency, urgency incontinence, voiding at night (nocturia), weak urinary stream, hesitency (needing to wait for the stream to begin), intermittency (when the stream starts and stops intermittently), straining to void, dysuria (burning sensation in the urethra), and dribbling
  • Mild prostate-related weak urinary stream: weak urinary stream
  • Missing testicle: Absence of a testicle
  • Moynahan syndrome I: A rare disorder characterized mainly by multiple moles, underdeveloped genitals, short stature, mental deficiency and heart defect. The moles cover virtually the whole body.
  • Multiple Sclerosis: Autoimmune attack on spinal nerves causing diverse and varying neural problems.
  • Multiple Sclerosis, Susceptibility To, 1: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 1 is linked to a defect on chromosome 6p21.3.
  • Multiple Sclerosis, Susceptibility To, 2: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 2 is linked to a defect on chromosome 10p15.1.
  • Multiple Sclerosis, Susceptibility To, 3: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 3 is linked to a defect on chromosome 5p13.2.
  • Multiple Sclerosis, Susceptibility To, 4: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 4 is linked to a defect on chromosome 1p36.
  • Mumps: An acute viral disease that causes the salivary glands to become swollen, sore and inflamed. Immunization had greatly reduced the incidence of this disease.
  • Naguib syndrome: A rare syndrome characterized mainly by wide-set eyes, hypospadias and extra fingers.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurofibromatosis-Noonan syndrome: A rare disorder where the patients has symptoms of neurofibromatosis (nerve tumors) and Noonan syndrome (short stature, bleeding problems, heart defect, unusual facial features, skeletal anomalies, webbed neck).
  • Non-Specific Urethritis: Urethral infection usually sexually transmitted
  • Noonan Syndrome: A rare genetic disorder characterized by a webbed neck, chest deformity, undescended testes and pulmonic stenosis.
  • Obal syndrome: The association of eye problems with severe malnutrition. The condition occurred frequently in soldiers, prisoners of war and people in concentration camps.
  • Occupational Cancer -- Bladder cancer: Occupational exposure to naphthylamine can increase the risk of developing bladder cancer.
  • Omodysplasia: A rare disorder characterized by short-limbed dwarfism, dislocated forearm and facial anomalies.
  • Omodysplasia type 1: A very rare syndrome characterized mainly by extremely short stature due to short bones in the arms and legs.
  • Oral facial digital syndrome, type 4: A rare inherited disorder characterized by facial, digital and oral abnormalities. Type IV is differentiated from the other types by the presence of severe shinbone deformity.
  • Orchitis: Inflammation of the testes.
  • Orstavik-Lindemann-Solberg syndrome: A rare disorder characterized by congenital heart defects, tongue tumors, extra fingers and webbing of fingers.
  • Osteogenesis imperfecta congenita, microcephaly, and cataracts: A rare genetic connective tissue disorder charactedrized by blue sclerae, cataracts and microcephaly - a lethal form of osteogenesis imperfecta.
  • Pain in the penis: penile pain may be due to the skin, muscle
  • Painful ejaculation: Painful ejaculation is a condition in which a man experiences discomfort when ejaculating.
  • Painful erection: Penis pain occurring from an erection
  • Painful urination: Painful urination refers to discomfort while urinating.
  • Paraphimosis: Retraction and constriction of the foreskin behind the glans penis.
  • Paroxysmal Nocturnal Hemoglobinuria: A condition which is characterized by the occurrence of hemoglobinuria at night without any identifiable cause.
  • Partial androgen insensitivity:
  • Partial deletion of Y: A very rare genetic disorder where a portion of chromosome Y is missing resulting in various abnormalities. Symptoms vary from case to case.
  • Pemphigus and fogo selvagem: An autoimmune skin disease characterized by skin blisters and a burning sensation. It is endemic particularly in Brazil but may also occur in other countries.
  • Penile Bruise: Bruise occurring on the penis.
  • Penile Burning Sensation: Burning sensation on the penis
  • Penile Itch: Sensation occurring on the penis that leads to a feeling of wanting to itch.
  • Penile Tingling: Tingling, prickling or pins and needles sensation occurring on or around the penis.
  • Penile cancer, adult: Cancer of the penis.
  • Penile rash: Rash occurring on the penis
  • Penile sores: A lesion present on the penis.
  • Penile tingling/ paresthesias: A tingling and numbness located in the penis
  • Penis blister: Small raised lesions in the eye less than 0.5mm in diameter.
  • Penis burning sensation: Abnormal sensation of burning felt along the penis.
  • Penis conditions: Any condition that affects the penis
  • Penis deformity: Distortion or malformation in the normal appearance of the penis.
  • Penis discharge: Fluid discharge from the penis
  • Penis infection: Infection of the penis.
  • Penis inflammation: Inflammation of the penis.
  • Penis lump: Raised irregular swelling of the penis.
  • Penis pain: Pain experienced within or on the skin of the penis.
  • Penis rash in children: Penis rash in children refers to an eruption or reaction on the surface of a child's penis.
  • Penis redness: Redness of the penis.
  • Penis sensitive: Increased sensitivity along the penis to external stimuli.
  • Penis swelling: Swelling of the penis
  • Penis symptoms: Various symptoms affecting the male penis
  • Penis tourniquet syndrome: Symptoms caused by putting a tight ring on the penis.
  • Penis ulcer: A local defect in the skin occurring on the penis.
  • Persistent painful erection: known as priapism
  • Peyronie's disease: Hard lump on the penis often causing bending.
  • Phimosis: Where there is constriction of the male foreskin so that it cannot be pulled back over the glans of the penis
  • Pierson syndrome: A very rare syndrome characterized mainly by a small pupil and kidney disease at birth.
  • Pituitary tumors, adult: A benign or cancer tumor that develops in the tissue of the pituitary gland in adults. The pituitary gland produces various hormones and some pituitary tumors (functioning tumors) can affect the secretion of one or more of these hormones resulting in a range of symptoms depending on the exact location of the tumor. Some pituitary tumors do not affect hormone production (nonfunctioning tumors).
  • Polyarteritis nodosa: A serious blood vessel disease where small and medium-sized arteries become swollen and damaged and are unable to adequately supply oxygenated blood to various tissues in the body. The disease can occur in a mild form or a serious, rapidly fatal form.
  • Polydactyly visceral anomalies cleft lip palate: A rare syndrome characterized mainly by the association of extra digits, cleft lip and/or palate and visceral anomalies. Various other abnormalities may also be present.
  • Polymicrogyria -- turricephaly -- hypogenitalism: A very rare syndrome characterized mainly by abnormal brain structure (polymicrogyria), cone shaped head and underdeveloped genitalia.
  • Polysyndactyly -- cardiac malformation: A very rare syndrome characterized mainly by an extra toe, webbed fingers and heart malformations.
  • Prader-Willi syndrome: A rare genetic disorder characterized by reduced muscle tone, obesity and small hands and feet.
  • Premature ejaculation: Ejaculation, usually with an orgasm, occuring before it is desired by the person, his partner or both.
  • Priapism: Sustained erection that lasts longer than 4 hours.
  • Primary prostate cancer: Prostate cancer is one of the most common cancers among males and is the second leading cause of cancer-related death in males.
  • Prolactinoma: Benign cancer of the pituitary gland producing prolactin.
  • Prolactinoma, familial: A pituitary tumor that secretes prolactin and occurs in a familial pattern of inheritance. The tumor is benign but can cause symptoms due to high prolactin levels or compression of the optic nerve.
  • Prostate Cancer: Cancer of the prostate.
  • Prostate bleeding: Bleeding in the prostate which usually occurs due to trauma.
  • Prostate blister: Raised small fluid filled lesions less than 0.5mm in diameter.
  • Prostate blockage like symptoms: conditions which cause symptoms similar to that when there is a blockage to prostate secretions
  • Prostate bruise: Usually occurs due to trauma.
  • Prostate burning sensation: Usually occurs due to urinary tract infection.
  • Prostate cancer, familial: An inherited form of prostate cancer where cancer cells develop in the prostate tissue in males.
  • Prostate cancer, hereditary, 1: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 1 is linked to a defect on chromosome 1q24-q25 and is inherited in a dominant manner.
  • Prostate cancer, hereditary, 10: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 10 is linked to a defect on chromosome 8q24.
  • Prostate cancer, hereditary, 11: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 11 is linked to a defect on chromosome 17p12.
  • Prostate cancer, hereditary, 12: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 12 is linked to a defect on chromosome 2p15.
  • Prostate cancer, hereditary, 13: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 13 is linked to a defect on chromosome 10q11.2.
  • Prostate cancer, hereditary, 14: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 14 is linked to a defect on chromosome 11q13.
  • Prostate cancer, hereditary, 15: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 15 is linked to a defect on chromosome 19q13.4.
  • Prostate cancer, hereditary, 2: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 2 is linked to a defect on chromosome 17p11.
  • Prostate cancer, hereditary, 3: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 3 is linked to a defect on chromosome 20q13.
  • Prostate cancer, hereditary, 4: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 4 is linked to a defect on chromosome 7p11-q21.
  • Prostate cancer, hereditary, 5: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 5 is linked to a defect on chromosome 3p26.
  • Prostate cancer, hereditary, 6: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 6 is linked to a defect on chromosome 22q12.3.
  • Prostate cancer, hereditary, 7: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 7 is linked to a defect on chromosome 15q12.
  • Prostate cancer, hereditary, 8: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 8 is linked to a defect on chromosome 1q42.2-q43.
  • Prostate cancer, hereditary, 9: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 9 is linked to a defect on chromosome 17q21-q22.
  • Prostate cancer, hereditary, X-linked 2: Many forms of prostate cancer are due to inherited defect on a chromosome. X-linked type 2 is linked to a defect on chromosome Xp11.22.
  • Prostate conditions/benign prostatic hyperplasia:
  • Prostate deformity: Distortion in the normal appearance of the prostate
  • Prostate disorder: prostate is a small gland that is located just below the bladder and surrounds the urethra. Along with the seminal vesicles it produces part of the semen
  • Prostate infection: Infection of the prostate gland.
  • Prostate inflammation: Any inflammation which occurs in the prostate
  • Prostate itch: Abnormal sensation felt in the prostate gland.
  • Prostate lump: Raised small swelling of the prostate.
  • Prostate pain: Pain that is located anatomically in the prostate
  • Prostate pain symptoms: conditions which causes pain similar to that of pain due to a prostatic pathology
  • Prostate rash: Change of the skin of the prostate which affects its colour, appearance or texture in the groin area.
  • Prostate redness: Usually occurs due to infection.
  • Prostate swelling: Usually occurs due infection.
  • Prostate symptoms: Symptoms of the male prostate gland
  • Prostate ulcer: Discontinuity in the lining epithelium of the prostate.

Conditions listing medical symptoms: Male sexual symptoms:

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Conditions listing medical complications: Male sexual symptoms:

The following list of medical conditions have 'Male sexual symptoms' or similar listed as a medical complication in our database.

 

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