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Symptoms » Fertility symptoms » Glossary
 

Glossary for Fertility symptoms

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

  • 17-Beta-hydroxysteroid dehydrogenase III deficiency: A rare disorder characterized caused by an enzyme (17-ketosteroid reductase) defect only in the testes which results in a lack of testosterone which is needed during the fetal stage to give males there physical characteristics.
  • 3-M Syndrome: A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected.
  • 46,XX Gonadal dysgenesis epibulbar dermoid: A rare disorder characterized by gonad abnormalities and an eye disorder called epibulbar dermoid.
  • 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.
  • 46,XY Gonadal Dysgenesis, Complete, SRY-Related: A rare disorder where a female has all the normal external femal characteristics but has non-functioning gonads. This means that no sex hormones needed for puberty are produced. This particular type is the result of a defect in the SRY gene located on chromosome Yp11.3.
  • 47,XXX syndrome: A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomatic.
  • APECED Syndrome: APECED is a recessively inherited genetic disease characterized by the presence of two of the following three conditions: impaired parathyroid function, yeast infection (candidiasis) and impaired adrenal gland function (Addison's disease). It is an autoimmune disease resulting from a genetic defect. The body's immune system malfunctions and attacks it's own body tissues.
  • Abdominal Cancer: Growth of abnormal cells (tumour) affecting the organs in the abdominal cavity; may be due to primary growth of a tumour or spread from another tumour (metastases, secondary tumour)
  • Acute epididymitis:
  • Acute herpes-like penile ulcers: formation of vesicles similar to the presentation in herpes
  • Acute oophoritis:
  • 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:
  • Adnexal tenderness: Tenderness of the appendages or secondary structures of the uterus.
  • Adolescent cataract and infertility syndrome: A rare syndrome characterized mainly by cataracts and infertility in male adolescents.
  • Adrenal Cancer: A malignant cancer that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids. Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
  • Adrenal Cortex Diseases: Diseases of the adrenal cortex. Examples includes Addison's disease, Cushing's syndrome and adrenal fatigue.
  • Adrenal Hyperplasia, Congenital (General): Congenital adrenal hyperplasia is an inherited condition characterized by adrenal insufficiency. It is caused by a deficiency in an enzyme needed to produce certain adrenal hormones such as cortisol and aldosterone.
  • Adrenal adenoma, familial: A benign tumor that develops in the adrenal gland and tends to run in families. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids . Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
  • Adrenal gland hyperfunction: Excessive activity of the adrenal gland which causes excessive production of one or more adrenal hormones (aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine). The increased adrenal gland activity may be caused by an adrenal gland tumor or by excessive stimulation of the gland. Pituitary hormones stimulate adrenal gland activity.
  • Adrenal hyperplasia, congenital type 3: A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency.
  • Adrenal hypoplasia congenital, X-linked: A genetic disorder which affects the body tissues that produce hormones. It is characterized by underdeveloped adrenal glands which results adrenal insufficiency and hypogonadotrophic hypogonadism.
  • Adrenal incidentaloma: A tumor of the adrenal gland that is discovered incidentally while performing an imaging examination for reasons other than an adrenal tumor. The tumor may be asymptomatic or can causes excessive secretion of adrenal hormones and resulting symptoms. The tumor may also be malignant or benign.
  • Adrenocortical carcinoma: A condition which is characterized by malignancy which affects the adrenocortex.
  • 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.
  • Adverse reaction to chemical -- 1,2-Dibromo-3-Chloropropane: 1,2-Dibromo-3-Chloropropane is a chemical used in soil fumigants and as a nematocide for various field crops. Commercial examples include Fumagon, Nemagon, Fumazone, Nemapax, Nemafume. Some people can suffer an adverse reaction to the chemical. The severity of symptoms varies depending on the amount of chemical involved and the route of exposure.
  • Aging: The medical conditions from getting older.
  • Ahumada-Del Castillo Syndrome: A form of secondary amenorrhea often resulting from a pituitary gland tumor. The condition causes galactorrhea and amenorrhea even when the patient is not pregnant.
  • Alagille syndrome: A genetic disorder affecting the liver and characterized by the absence of some or all of the liver bile ducts that transport bile within the liver.
  • Alopecia -- hypogonadism -- extrapyramidal disorder: A rare syndrome characterized by alopecia, progressive movement problems and a lack of gonadal function which affects puberty.
  • 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.
  • Anophthalmia -- hypothalamo-pituitary insufficiency: A rare syndrome characterized mainly by small or absent eyes and malformations of the hypothalamus and pituitary gland.
  • Anophthalmia -- hypyothalamo-pituitary insufficiency: A rare syndrome characterized mainly by small or absent eyes and malformations of the hypothalamus and pituitary gland.
  • Anophthalmia -- microcephaly -- hypogonadism: A rare syndrome characterized mainly by absent eyes, a small head and hypogonadism.
  • Anorchia: Congenital condition where one or both testes are absent.
  • 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.
  • Anterior pituitary hyperhormonotrophic syndrome: A syndrome characterized by the excessive production of various hormones (gonadotrophic, thyrotrophic, lactotrophic and pancreatrophic hormone).
  • Appendiceal tumor: A tumor of the appendix. The condition is often misdiagnosed as acute appendicitis. The cancer usually metastasizes from other sites and rarely starts in the appendix.
  • Appendix cancer: Cancer of the appendix. The cancer usually metastasizes from other sites and rarely starts in the appendix.
  • Aromatase deficiency: A congenital deficiency of the enzyme called aromatase which is needed to convert androgens to estrogens.
  • Asherman Syndrome: A condition where adhesions form inside the uterus because of uterine surgery or infection. The adhesions may cause menstruation to cease and/or infertility.
  • Asherman's syndrome: Scarring and adhesions that develop in the uterus and can result in menstrual and fertility problems.
  • Attenuated congenital adrenal hyperplasia: A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as childhood.
  • Autoimmune Endometriosis: An endometriosis that is caused by an autoimmune reaction
  • Autoimmune Hypophysitis: Inflammation of part of the pituitary gland due to an autoimmune process resulting in impaired pituitary hormone production. The range and severity of symptoms is variable depending on the degree of damage to the pituitary gland.
  • Autoimmune oophoritis: An autoimmune condition where the body's own immune system attacks the ovaries and causes them to become inflamed. It can lead to ovarian function stopping prematurely.
  • Autoimmune thyroid disease associated Celiac Disease: Patients with autoimmune thyroid disease are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
  • Autoimmune thyroid diseases: Autoimmune diseases of the thyroid gland.
  • Azoospermia: Total lack of sperm in ejaculate
  • Bacterial prostatitis: Bacterial prostatitis is a bacterial inflammation of the prostate gland, in men.
  • 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.
  • Benign ovarian cyst:
  • Benign prostate hypertrophy: Non-cancerous prostrate enlargement common with aging
  • Bent penis: Abnormal bending or curvature of the penis
  • Biemond syndrome type 2: A rare inherited condition characterized by mental retardation, obesity, polydactyly and underdeveloped genitals.
  • Bilateral adnexal tenderness: grave gynaecological complication
  • Birth symptoms: Symptoms related to childbirth.
  • 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.
  • Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome, type 1: A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid. The severity of symptoms is variable. There are two subtypes of the condition: Type 2 involves eye anomalies as well as female fertility problems whereas type 1 only involves the eye anomalies.
  • Bloody ejaculation: Blood appearing in the ejaculate after male ejaculation
  • Bloody semen: Blood appearing in ejaculated semen
  • Bloom Syndrome: A rare genetic inherited genetic disorder which mainly affects Ashkenazic Jewish people and is characterized by short stature, malar hypoplasia, and a telangiectatic erythema of the face.
  • Boggy enlarged prostate: enlarged painful prostate
  • Borjeson Syndrome: A rare genetic disorder characterized by severe mental deficiency, large ears, hypogonadism and other abnormalities.
  • Borjeson-Forssman-Lehmann 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.
  • Bronchiectasis -- oligospermia: A rare syndrome characterized by the association of bronchiectasis (enlarged bronchial airways) and a defect in the sperm ducts which affects the number of sperm produced. Patients suffer frequent bacterial infections.
  • CCFDN: A rare, recessively inherited syndrome characterized by cataracts during infancy, unusual facial appearance and neuropathy.
  • CDG syndrome type 1A: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • CDG syndrome type I: A rare genetic disorder where the body is unable to synthesize glycoproteins which results in multisystem problems.
  • Calloso-genital dysplasia: A rare syndrome characterized by the total absence of the brain structure that connects the two halves of the brain (corpus callosum) as well as absent menstruation and coloboma.
  • Camera-Marugo-Cohen syndrome: A rare syndrome characterized mainly by mental retardation, muscle weakness, obesity and an asymmetrical body.
  • Camurati-Engelmann Disease: A very rare genetic disease thickening of areas of bone causing pain, weakness and wasting. Usually affects the legs during childhood. Also called diaphyseal dysplasia.
  • 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 deafness hypogonadism: A very rare syndrome characterized mainly by deafness, cataracts and a deficiency of sex hormone production.
  • Cephalopolysyndactyly: A rare genetic disorder characterized by premature closing of skull bones and craniofacial abnormalities, finger and toe abnormalities. The type and severity of symptoms is variable with many cases remaining undiagnosed because their condition is relatively mild and doesn't cause many problems.
  • 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.
  • Cervicitis: A condition which is characterized by inflammation of the cervix
  • Chemical poisoning -- 1,2-Dibromo-3-Chloropropane: 1,2-Dibromo-3-Chloropropane is a chemical used in soil fumigants and as a nematocide for various field crops. Commercial examples include Fumagon, Nemagon, Fumazone, Nemapax, Nemafume. Excessive exposure to this chemical can cause relatively mild symptoms. The chemical may be absorbed through the skin. The severity of symptoms varies depending on the amount of chemical involved and the route of exposure.
  • Chemical poisoning -- Chlordecone: Chlordecone is an insecticide used to control pests in crops such as bananas and tobacco. Ingestion and other exposures to the chemical can cause various symptoms. The chemical may be readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Lead-containing Paint: Lead pain contains lead as well as other harmful chemicals. The lead in the pain is toxic (especially to young children) and ingesting fresh or old paint can cause serious symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chiari-Frommel syndrome: A hormonal disorder where a woman continues to produce milk even after the child has been weaned.
  • Chlamydia: Common sexually transmitted disease often without symptoms.
  • Chromosome 13p duplication: A rare chromosomal disorder where duplication of a portion of chromosome 13 causes various abnormalities such as mental retardation, short stature, facial dysmorphism, delayed puberty and heart defects.
  • Chromosome 15 Ring: A rare chromosomal disorder where genetic material from one or both ends of chromosome 15 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 15q duplication syndrome: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
  • Chromosome 15q, partial deletion: A rare chromosomal disorder involving deletion of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the deleted genetic material.
  • Chromosome 15q, trisomy: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
  • Chromosome 3, monosomy 3p: A rare chromosomal disorder where a portion of chromosome 3 is absent and is characterized by mental and growth deficiency, drooping upper eyelid and polydactyly.
  • 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 6p deletion syndrome: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 6 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome Y deletion: An inherited chromosomal disorder where the deletion of the chromosome results in male infertility.
  • 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 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
  • Chronic renal insufficiency: Chronic lack of function of the renal system. Kidneys.
  • Chudley syndrome 1: A rare syndrome characterized by mental retardation, obesity, hypogonadism and a distinctive mouth.
  • Ciliary dyskinesia, due to transposition of ciliary microtubules: A very rare disorder where the cilia fail to move adequately due to abnormal cilia structure. The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Cirrhosis of liver: diffuse hepatic process characterized by fibrosis and the conversion of normal liver architecture into structurally abnormal nodules
  • Collagenous celiac disease: Collagenous celiac disease is used to describe progressive celiac disease characterized by the presence of a layer of collagen (scarring) in the intestinal layers. This form of celiac disease usually fails to respond to treatments such as gluten-free diets. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition usually fails to respond to treatment and has a poor prognosis.
  • Complete androgen insensitivity:
  • Congenital Disorders of Glycosylation Type Ia: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • Congenital adrenal hyperplasia -- non-classical form: A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as childhood.
  • 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 bilateral absence of vas deferens:
  • Congenital bilateral aplasia of vas deferens: A birth defect where the tubes that carry sperm from the testes to the penis don't develop.
  • Congenital disorder of glycosylation type 1A: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • Congenital disorder of glycosylation type 1K: 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 Ik is caused by a defect on chromosome 16p13.3 and involves a defect in the gene for beta-1,4-mannosyltransferase. The disorder is generally fatal within a year or two of birth.
  • 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.
  • Corpus luteum hematoma: Corpus luteum hematoma is a collection of blood in a woman's ovary.
  • Cortisone reductase deficiency: An inborn error of steroid metabolism due to a deficiency of an enzyme called cortisone reductase (11-beta-hydroxysteroid dehydrogenase). This enzyme is needed to convert cortisone to cortisol.
  • Cryptorchidism in children: Cryptorchidism in children refers to a boy who has an undescended testicle.
  • Cushing syndrome, familial: A hormonal disorder caused by high levels of the cortisol hormone due to the abnormal development of the adrenal gland.
  • Cushing's disease: A condition of hyperadrenocorticism which is secondary to excessive pituitary secretion of ACTH. Cushing's disease is different to Cushing's syndrome which refers to the effects of glucocorticoid excess from any cause.
  • Cushing-like symptoms: Symptoms similar to those of Cushing's disease
  • 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 Sanctis-Cacchione syndrome: A rare genetic ectodermal disorder characterized by sunlight sensitivity, skin atrophy and pigmentation and skin tumors as well neurologic involvement.
  • 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 hypogonadism syndrome: A rare condition characterized by the combination of hypogonadism and deafness.
  • Decreased penile sensation: Decreased penile sensation is a lowered level of feeling in the penis.
  • Del Castillo's syndrome: Infertility due to absence of germinal cells which are needed to make sperm.
  • Delayed ejaculation: A condition which is characterized by a delay in the males ability to ejaculate
  • Delayed puberty: A lack of sexual maturation in an adolescent at an age significantly higher than the average age that child of that epidemiology attains puberty.
  • Delayed sexual development: Delayed sexual development refers to late development of the sexual organs.
  • Deletion 3p: A rare chromosomal disorder where a portion of chromosome 3 is absent and is characterized by mental and growth deficiency, drooping upper eyelid and extra digits.
  • Dermoid cyst: Benign cystic tumor often containing skin, hair, and other tissue
  • Diabetes-like symptoms: Symptoms similar to those of diabetes
  • Diethylstilbestrol: A synthetic nonsteroidal estrogen
  • Diethylstilbestrol antenatal exposure: Abnormalities and defects that can occur in an infant exposed to diethylstilbestrol (a medication used to prevent complications during pregnancy such as miscarriage and prematurity) during pregnancy. The syndrome
  • Diethylstilbestrol antenatal infection: A very rare syndrome characterized mainly caused by exposure to diethylstilbestrol (used to prevent complications during pregnancy such as miscarriage and prematurity) during pregnancy
  • Discharge from penis: abnormal discharge from the penis which is not urine or semen
  • Disorders of the ovaries:
  • Disorders of the uterus in the reproductive age group:
  • Down Syndrome: A chromosome syndrome causing physical effects and mental retardation.
  • Down's syndrome associated Celiac Disease: Patients with Down's syndrome have a high degree of susceptibility to developing celiac disease. Up to 17% of Down's syndrome sufferers develop celiac disease but this rate varies amongst age groups and country of origin. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
  • Dup (2) (pter-p13)): 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 though early death is quite common.
  • Dysfunctional Uterine Bleeding: Uterus bleeding unrelated to periods
  • Dysmenorrhea: Excessive menstrual-like cramping pain
  • Early puberty: Early puberty refers to an premature onset of the physical changes in the body that signal readiness for reproduction.
  • 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.
  • 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
  • Endometrial conditions: Conditions that affect the female endometrium that is located in the uterus
  • Endometriosis: Misplaced uterus tissue causing scar tissue.
  • Endometritis: Inflammation of the endometrium (uterine lining)
  • Enlarged ovaries: Where the ovaries of a female have increased in size to what is considered normal
  • Enlarged ovary: An enlargement of the female ovary to a size bigger than considered normal
  • Enlarged testicle: Enlargement of the male testicle to a size considered to be more than normal
  • Epididymal nodules: presence of nodules in the epididymis
  • Epididymo-orchitis: A condition which is characterized by inflammation of the epididimis and testes of a male
  • Erectile dysfunction: The inability to obtain on normal erection
  • Face symptoms: Symptoms affecting the face
  • Factor XIII Deficiency: A very rare inherited or acquired blood disorder caused by a deficiency of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems.
  • Factor XIII deficiency, congenital: A very rare inherited blood disorder caused by a deficiency of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems.
  • Factor XIII, A1 subunit Deficiency: A very rare inherited or acquired blood disorder caused by a deficiency of subunit A of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems.
  • Factor XIII, B subunit Deficiency: A very rare inherited or acquired blood disorder caused by a deficiency of subunit B of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems.
  • Fallopian tube conditions: Conditions that affect the fallopian tubes of a woman
  • Fallopian tube symptoms: Symptoms affecting the female fallopian tubes
  • Familial hypopituitarism: Impaired pituitary gland hormone-producing activity that tends to run in families. The failure of the pituitary gland in turn affects other hormone-producing glands which rely on the hormones from the pituitary gland for their activity. Symptoms are determined by the degree and type of hormone deficiency involved.
  • Female genital disorders: Any condition affecting the female genital organs.
  • Female genital organ tumors: Tumors affecting the female genital organs, whether cancerous or bening.
  • Female infertility: A condition characterized by the inability of a female to become pregnant
  • Female pseudohermaphrodism -- anorectal anomalies: A very rare disorder characterized by ambiguous external genitals and anal and rectal anomalies.
  • Female reproductive symptoms: Symptoms affecting the female reproductive organs.
  • Female reproductive toxicity: There is mounting evidence which indicates that exposure to certain agents may produce adverse reproductive or fetal developmental effects. The possible range of effects includes reduced fertility, low birth weight, childhood cancer, spontaneous abortion and birth defects. Agents which may be implicated in these adverse effects includes anticancer drugs, carbon disulfide, carbon monoxide, lead, pesticides, organic solvents and tobacco smoke.
  • Fertile eunuch syndrome: A rare condition where hypogonadism is not severe enough to cause total infertility by may cause reduced infertility. The condition involves reduced amounts of luteinizing hormone-releasing hormone.
  • Fertility conditions: Medical conditions relating to fertility, including infertility.
  • Follicle-stimulating hormone deficiency, isolated: A genetic disorder characterized by the deficiency of follicle-stimulating hormone which primarily affects fertility.
  • Forbes-Albright syndrome: A rare condition where a hormone secreting pituitary or hypothalamic tumor causes galactorrhea and amenorrhea.
  • 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
  • Fowler-Christmas-Chapple syndrome: A rare syndrome characterized by the association of polycystic ovaries with the abnormal functioning of the urinary valve.
  • Freire-Maia odontotrichomelic syndrome: A rare syndrome characterized by tooth, hair and limb abnormalities.
  • Freire-Maia syndrome: An extremely rare syndrome characterized by tooth, hair and limb abnormalities. The abnormalities can be quite severe in some cases. The parents may have been related in the reported cases.
  • GAPO syndrome: A rare condition characterized by retarded growth, alopecia, otpic atrophy and failure of teeth to erupt.
  • Galactorrhea: This is where there is an excessive or spontaneous flow of milk from the female breast
  • Galactorrhoea-Hyperprolactinaemia: Increased blood prolactin levels associated with galactorrhea (abnormal milk secretion). It may be caused by such things as certain medications, pituitary disorders and thyroid disorders. The condition can occur in males as well as females.
  • Gelatinous ascites: A large abdominal cyst filled with gelatinous or mucous fluid. It is often caused by a mucous-producing abdominal cancer.
  • 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.
  • 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.
  • Gloomy syndrome: A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected.
  • Gonadal dysgenesis: The abnormal development of gonads which means that the sex hormones are not being produced. The gonads are the primary reproductive organs - testes in males and ovaries in females. These organs produced sperm and eggs as well as sex hormones - testes produce the male hormone called testosterone and ovaries produce the female hormone called estrogen. Abnormal gonad development and hence lack of sex hormones can affect sexual differentiation between males and females and puberty may be delayed or fail to occur altogether.
  • Gonadal dysgenesis Turner type: The abnormal development of gonads that occurs in Turner syndrome due to a chromosomal abnormality. It occurs when the there is only one fully functioning X chromosome instead of two which results in underdeveloped female characteristics. The severity of symptoms is determined by how much of the second sex chromosome is missing.
  • Gradual onset of scrotal swelling: Gradual onset of scrotal swelling is a slow development of puffiness or abnormal enlargement of the scrotum.
  • Grahmann's syndrome: Abnormal development of the part of the brain called the diencephalon which in turn affects the pituitary gland. The main manifestations are impaired sexual development, obesity and periodic psychotic episodes.
  • Granulomatous hypophysitis: A rare disorder caused by the inflammation of the pituitary gland. It can occur as a result of other infections such as tuberculosis and sarcoidosis.
  • Graves disease: A condition which is an autoimmune disease that affects the thyroid resulting hyperthyroidism
  • Greig Cephalopolysyndactyly Syndrome: A rare genetic disorder characterized by premature closing of skull bones and craniofacial abnormalities, finger and toe abnormalities.
  • Gynaecological conditions: Any condition the affects the female reproductive organs
  • HAIR-AN Syndrome: A very rare syndrome that affects females only and is characterized mainly by insulin resistance, dark velvety patches of skin and increased male hormone production in females.
  • Harper dwarfism: A rare inherited disorder involving a range of abnormalities. It is a variant of the Seckel syndrome.
  • Hashimoto's thyroiditis: Hashimoto thyroiditis is characterized by the destruction of thyroid cells by various cell- and antibody-mediated immune processes. Patients with Hashimoto thyroiditis have antibodies to various thyroid antigens, the most frequently detected of which include antithyroid peroxidase (anti-TPO), antithyroglobulin (anti-Tg), and, to a lesser extent, TSH receptor-blocking antibodies.
  • Head symptoms: Symptoms affecting the head or brain
  • Heller-Nelson syndrome: A variant of Klinefelter syndrome (extra X chromosome in most cells) involving a range of abnormalities.
  • 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."
  • Hereditary hypothyroidism: Hereditary hypothyroidism is a condition in which there is a defect in the thyroid gland which leads to increased production of TSH reduced production of thyroid hormone.
  • Hermaphroditism: A very rare genetic disorder where a baby is born having both male and female internal sex organs.
  • Herpes-like penile ulcers: formation of vesicles similar to the presentation in herpes
  • Hirsutism in polycystic ovarian disease: Hirsutism in polycystic ovarian disease is a condition in which there is an excessive growth of dark hair in unusual places on a female's body, such as on the face, that is caused by polycystic ovarian disease.
  • Hodgkin's disease, adult: A type of cancer that affects the lymphatic system in adults. The lymphatic system forms part of the body's immune system. This type of cancer can also occur in children.
  • Hodgkin's disease, childhood: A type of cancer that affects the lymphatic system in children. The lymphatic system forms part of the body's immune system. This type of cancer can also occur in children.
  • Hyperadrenalism: Excessive levels of adrenal hormones in the body. Symptoms depend on which hormone is involved and the degree of involvement. Adrenal hormones are aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine.
  • Hyperandrogenism: Excessive levels of androgen (male sex hormones) that can occur in males and females.
  • Hypergonadotropic ovarian failure: Premature onset of menopause - occurs before the fourth decade -average age of onset of menopause is about 50 years of age. The condition can occur sporadically or may be inherited in a familial manner.
  • Hypergonadotropic ovarian failure, familial or sporadic: A rare disorder where the ovaries fail to function prematurely. Ovarian failure can occur in the 20's or 30's. Normal ovarian failure occurs during menopause. Premature ovarian failure can be caused by a genetic mutation and can occur sporadically or in a familial pattern.
  • 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
  • Hyperthyroidism: The excessive activity of the thyroid gland
  • Hypogonadism: medical term for a defect of the reproductive system that results in lack of function of the gonads (ovaries or testes).
  • Hypogonadism -- mitral valve prolapse -- mental retardation: A very rare syndrome characterized mainly by a heart disorder, hypogonadism and mental retardation.
  • 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.
  • Hypoparathyroidism X-linked: Low parathyroid levels inherited in a X-linked manner and hence only males are symptomatic and females are asymptomatic carriers.
  • Hypopituitarism: A condition characterized by diminished hormonal section by the pituitary gland
  • Hypothalamic amenorrhea: A condition which is characterized by amenorrhea caused by a an abnormality of the hypothalamus
  • Hysterectomy: The surgical removal of the female uterus
  • Ichthyosis male hypogonadism: A very rare syndrome characterized mainly by scaly skin and insufficient hormone production by the male gonads.
  • Immotile cilia syndrome, due to defective radial spokes: A very rare disorder where the cilia fail to move adequately due to abnormal cilia structure. The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility.
  • Immotile cilia syndrome, due to excessively long cilia: A very rare disorder where the cilia fail to move adequately due to abnormally long cilia. The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Impotence: Difficulty starting or maintaining an erection
  • Induration of the prostate: swelling of the prostate gland
  • Infantile hypothyroidism: A condition in infancy or early childhood due to an in-utero deficiency of thyroid hormones that can be caused by genetic or environmental factors, such as thyroid dysgenesis or hypothyroidism in infants of mothers treated with thiouracil during pregnancy.
  • Infertility: Inability of couples to establish pregnancy by having sexual intercourse over a period of time, usually more than 1 year in length.
  • 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
  • Irritation of scrotum skin: A condition which is characterized by irritation of the skin of the scrotum
  • 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.
  • Keratoderma -- epithelioma -- dental abnormalities- hypogonadism: A rare disorder characterized by skin and dental abnormalities as well as hypogonadism.
  • 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.
  • Late start of menstruation: Late first period in adolescent girls
  • Laurence-Moon Syndrome: A rare inherited disorder characterized by vision loss, impaired hormone production, mental retardation and spastic paraplegia.
  • Lead poisoning: A type of heavy metal poisoning caused by excessive exposure to lead.
  • 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.
  • Light periods: Unusually light menstrual bleeding
  • Lipoid congenital adrenal hyperplasia: A rare form of congenital adrenal hyperplasia where the early phase of adrenal cortisol production is defective which causes mineralocorticoid deficiency. Male pseudohermaphroditism is the main characteristic of this disorder.
  • Liver symptoms: Symptoms affecting the liver
  • Low-level radiation exposure: Tissue injury can result from exposure to radiation. The radiation dose, rate of dosing and tissues irradiated will determine the severity and type of symptoms. The effects may be chronic, delayed or acute. Low-level radiation is usually associated with delayed effects.
  • 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.
  • Luteinizing hormone releasing hormone, deficiency of, with ataxia: A very rare syndrome characterized mainly by insufficient sex hormone production and impaired balance and coordination due to nervous system dysfunction.
  • Male genital symptoms: Symptoms affecting the male genitals.
  • Male impotence: it is most poorly understood and mismangaed of all medical disorders. Can be divided into primary and secondary
  • Male infertility: When a male is not able to produce offspring
  • Male reproductive conditions: Medical conditions affecting the male reproductive system.
  • Male reproductive symptoms: Symptoms affecting the male reproductive organs.
  • Male reproductive toxicity -- 1,2-Dibromo-3-Chloropropane (DBCP): Exposure to 1,2-Dibromo-3-Chloropropane (DBCP), a recognized reproductive toxicant, can negatively affect the male reproductive system. 1,2-Dibromo-3-Chloropropane (DBCP) is used mainly as an ingredient in pesticides such as Fumazone and Nemagon. The severity and nature of the adverse effect is variable and can be influenced by factors such as level of exposure and individual sensitivity to the chemical. Effects on the male reproductive system can include such things as altered sexual behavior, altered fertility and problems with sperm shape or count.
  • Marijuana abuse: Illicit depressant/hallucinogenic drug
  • Marijuana addiction: Marijuana addiction is the uncontrollable desire to use marijuana on a regular basis. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
  • Martsolf syndrome: A rare inherited condition characterized by mental retardation, cataracts, small head and hypogonadism (reduced production of hormones by ovaries or testes).
  • Masculinisation: Increased male physical appearance in females
  • Medication related hypothyroidism: Drug-induced hypothyroidism is an underactive thyroid gland due to a reaction from medication.
  • Meier-Rotschild syndrome: A rare disorder characterized mainly by short stature, small ears and absent kneecaps.
  • Menopause: End of female reproductive years
  • Menopause symptoms: Symptoms similar to menopause or closely related.
  • Mental retardation -- dysmorphism -- hypogonadism -- diabetes: A very rare syndrome characterized mainly by mental retardation, hypogonadism, diabetes and facial and skull abnormalities.
  • Mental retardation -- epileptic seizures -- hypogonadism -- hypogenitalism -microcephaly -- obesity: A very rare syndrome characterized mainly by mental deficiency, epilepsy, small head, small genitals and obesity. Death occurs within the first two years of life.
  • Mental retardation X-linked syndromic 7: A very rare syndrome characterized mainly by mental retardation, obesity, hypogonadism and tapered fingers.
  • Mental retardation, X-linked -- hypogonadism -- ichthyosis -- obesity -- short stature: A rare X-linked disorder characterized by mental retardation, obesity, short stature, hypogonadism and a skin disorder. 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 -- hypotonic face: A group of syndromes characterized mainly by mental retardation and reduced tone in the facial muscles. Various other abnormalities may be present.
  • Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity: A very rare syndrome characterized mainly by mental deficiency, epilepsy, small head, small genitals and obesity. Death occurs within the first two years of life.
  • Microcephaly -- hypergonadotropic hypogonadism -- short stature: A very rare syndrome characterized mainly by a small head, short stature and hypogonadism.
  • 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
  • Moebius axonal neuropathy -- hypogonadism: A very rare syndrome characterized mainly by facial paralysis due to problems with 6th and 7th nerve development (Moebius sequence) and hypogonadism.
  • 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.
  • Muckle-Wells syndrome: An inherited condition characterized by amyloidosis (protein deposits), deafness, hives and limb pain.
  • Mullerian derivatives, persistent: A very rare syndrome where a genetic defect results in the development of female organs in an otherwise normal male. The genetic defect causes a hormone deficiency (anti-mullerian hormone) which allows mullerian derivates, such as a uterus, to form in males.
  • Multiple endocrine abnormalities -- adenylyl cyclase dysfunction: A rare syndrome characterized by an enzyme defect (adenylyl cyclase) and a number of endocrine abnormalities.
  • Multiple endocrine neoplasia type 1: Rare inherited disease causing tumors in multiple glands
  • Multiple pterygium syndrome: A very rare disorder characterized by webbing of various parts of the body, contractures, short stature, fusion of neck vertebrae and facial anomalies.
  • Muscular dystrophy -- congenital infantile cataract -- hypogonadism: A very rare syndrome characterized mainly by muscle wasting, infantile cataracts and hypogonadism.
  • Muscular dystrophy, congenital, infantile with cataract -- hypogonadism: A very rare syndrome characterized mainly by muscle wasting, infantile cataracts and hypogonadism.
  • Myhre-Ruvalcaba-Kelley syndrome: A rare recessively inherited X-linked disorder characterized by hearing impairment from birth and hypogonadism.
  • Myoma (fibroid): A benign tumour of the muscle in the wall of the uterus.
  • Nathalie syndrome: A very rare condition described in four children of one family. The condition is characterized by wasting of the spine muscles, abnormal heart electrical activity, cataracts, hypogonadism and hearing impairment.
  • Nevi -- atrial myxoma -- myxoid neurofibromata -- ephelides: A very rare syndrome characterized by spotty pigmentation on the skin and the development of multiple benign tumors (myxoma) that can occur just about anywhere in the body but mainly in the skin, breast and heart and endocrine glands such as the thyroid and pituitary gland. The symptoms are highly variable depending on the location, size and number of tumors. Endocrine gland tumors can affect hormone production and hence result in a range of symptoms.
  • Nicotine addiction: Nicotine addiction is the uncontrollable desire to continue smoking. Smoking products contain nicotine which is a chemical that can lead to addiction if used over a period of time. Cessation causes withdrawal symptoms which can vary in nature and severity.
  • Non Classic Congenital Adrenal Hyperplasia: A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as childhood.
  • Non-Specific Urethritis: Urethral infection usually sexually transmitted
  • Occupational Cancer -- Bladder cancer: Occupational exposure to naphthylamine can increase the risk of developing bladder cancer.
  • Oligospermia: Abnormally small amount of spermatozoa in the semen.
  • Oophoritis: Oophoritis, also known as pelvic inflammatory disease, is an inflammation and infection of a woman's ovaries, often due to a sexually transmitted disease.
  • Orchitis: Inflammation of the testes.
  • Osteosclerosis -- ichthyosis -- premature ovarian failure: A very rare syndrome characterized mainly by increased bone density, scaly skin and premature menopause.
  • Osteosclerosis with ichthyosis and premature ovarian failure: A very rare syndrome characterized mainly by increased bone density, scaly skin and premature menopause.
  • Ovarian cancer: A condition which is characterized by a malignancy that is located in the ovary
  • Ovarian cyst: A cyst which is located in the ovary
  • Ovarian cysts: Cysts which are located in the ovaries
  • Ovarian insufficiency due to FSH resistance: A rare disorder where the ovaries fail to function normally as they are unable to respond to follicle stimulating hormones.
  • Ovarian insufficiency, familial: A rare inherited disorder where the ovaries fail to function normally despite normal levels of hormones that stimulate ovarian activity. Ovarian failure is a normal phase of aging and is associated with menopause but it is termed ovarian insufficiency when it occurs in a female under the age of 40.
  • Ovarian tumour: A tumour that is located on the ovary.
  • Ovary symptoms: Symptoms affecting the ovaries
  • 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
  • Panhypopituitarism: A rare condition where all pituitary hormones are absent or reduced. The condition may be congenital or acquired through such things as pituitary tumors. The pituitary gland regulates the activity of other endocrine glands as well as controlling growth. Other endocrine glands include adrenal, parathyroid, thyroid, pancreas, ovaries and testes. Symptoms can vary greatly depending on the degree of deficiency of the various hormones.
  • Partial androgen insensitivity:
  • Pelvic inflammatory disease: A condition which is characterized by an infection which is located in the upper female genital tract
  • 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 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 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 ulcer: A local defect in the skin occurring on the penis.
  • Perimenopause: The start of onset of menopause
  • Persistent painful erection: known as priapism
  • Phenylketonuria: A metabolic disorder where there is a deficiency of the enzyme phenylalanine hydroxylase which leads to a harmful buildup of the phenylalanine in the body. Normally the phenylalanine is converted into tyrosine. The severity of the symptoms can range from severe enough to cause mental retardation to mild enough not to require treatment. Severity is determined by the level of impairment of enzyme activity of phenylalanine hydroxylase.
  • Pituitary Cancer: Cancer of the pituitary gland.
  • Pituitary cancer, childhood: Cancer (malignant) of the pituitary gland in children. 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).
  • 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).
  • Polycystic ovarian disease, familial: A rare familial condition characterized by menstrual abnormalities, excessive growth of hair, obesity and infertility.
  • Polycystic ovaries urethral sphincter dysfunction: A rare syndrome characterized by the association of polycystic ovaries with the abnormal functioning of the urinary valve.
  • Polycystic ovary syndrome: Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects approximately 5% of all women.
  • Polyneuropathy -- mental retardation -- acromicria -- premature menopause: A very rare syndrome characterized mainly by premature menopause, sensory impairment, mental retardation and small, delicate facial bones.
  • Prader-Willi syndrome: A rare genetic disorder characterized by reduced muscle tone, obesity and small hands and feet.
  • Precocious puberty: Precocious puberty refers to a condition in which the maturing of the sex organs and the rest of the body occurs earlier than usual.
  • Precocious puberty in female children: Precocious puberty in female children refers to a girl in whom maturing of the sex organs and the rest of the body occurs earlier than usual.
  • Precocious puberty in male children: Precocious puberty in male children refers to a body in whom maturing of the sex organs and the rest of the body occurs earlier than usual.
  • Pregnancy symptoms: Symptoms related to pregnancy.
  • Premature ejaculation: Ejaculation, usually with an orgasm, occuring before it is desired by the person, his partner or both.
  • Premature ovarian failure, familial: A familial condition where menopause tends to occur before the fourth decade -average age of onset of menopause is about 50 years of age.
  • Priapism: Sustained erection that lasts longer than 4 hours.
  • Primary ciliary dyskinesia: A very rare disorder where the cilia fail to move. The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 10: A very rare disorder where the cilia fail to move. Type 10 differs from the other forms of primary ciliary dyskinesia in the location of the genetic defect (14q21.3). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 11: A very rare disorder where the cilia fail to move. Type 11 differs from the other forms of primary ciliary dyskinesia in the location of the genetic defect (6q22). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 12: A very rare disorder where the cilia fail to move. Type 12 differs from the other forms of primary ciliary dyskinesia in the location of the genetic defect (6p21.1). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 2: A very rare disorder where the cilia fail to move. Type 2 differs from the other forms of primary ciliar dyskinesia in the location of the genetic defect (19q13.3qter). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 3: A very rare disorder where the cilia fail to move. Type 3 differs from the other forms of primary ciliar dyskinesia in the location of the genetic defect (5p). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 4: A very rare disorder where the cilia fail to move. Type 4 differs from the other forms of primary ciliar dyskinesia in the location of the genetic defect (15q13.1-q15.1). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 5: A very rare disorder where the cilia fail to move. Type 5 differs from the other forms of primary ciliar dyskinesia in the location of the genetic defect (16p12.2-p12.1). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 6: A very rare disorder where the cilia fail to move. Type 6 differs from the other forms of primary ciliar dyskinesia in the location of the genetic defect (7p14-p13). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 7: A very rare disorder where the cilia fail to move. Type 7 differs from the other forms of primary ciliary dyskinesia in the location of the genetic defect (7p21). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 8: A very rare disorder where the cilia fail to move. Type 8 differs from the other forms of primary ciliary dyskinesia in the location of the genetic defect (15q24-q25). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary ciliary dyskinesia, 9: A very rare disorder where the cilia fail to move. Type 9 differs from the other forms of primary ciliary dyskinesia in the location of the genetic defect (17q25). The cilia are tiny, hair-like structures found in the respiratory and ear passages and help to clear debris and mucus. This results in increases risk of respiratory infections, sinusitis, ear infections and male infertility. The infertility results as the tails of sperm is basically cilia.
  • Primary cortisol resistance: A rare genetic disorder where the body is unable to respond to a hormone called cortisol. The body produces excess cortisol to compensate for this defect.
  • Primary hypothyroidism: Primary hypothyroidism is a condition in which a defect in the thyroid gland leads to reduced production of thyroid hormone.
  • 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 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 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.
  • Prostate-related urinary dribbling: weak urinary stream
  • 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
  • Prostate-related weak urinary stream: weak urinary stream
  • Prostatic enlargement: increase in the size of the prostate gland
  • Prostatic rigidity: feeling of rigidity on plapation of the prostate gland
  • Prostatic tuberculosis: Tuberculous prostatitis must be viewed as a systemic disease, and the treatment is primarily medical. Hospitalization is usually unnecessary but may be required to treat noncompliant patients.
  • Prostatitis: Inflammation of the prostate
  • Proximal myotonic dystrophy: A very rare genetic muscle disorder which is often associated with cataracts, abnormal heart rhythm and infertility. Muscle weakness tends to occur more in muscles closer to the trunk such as the neck, shoulders, hips and upper legs. Pregnancy can exacerbate or initiate symptoms.
  • Pseudohermaphrodism -- anorectal anomalies: A very rare disorder characterized by ambiguous external genitals and anal and rectal anomalies.
  • Psychiatric disorders associated Celiac Disease: Patients with Psychiatric disorders are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
  • Pubertal delay in children: Pubertal delay in children refers to a child who has a delay in the maturing of sexual characteristics.
  • Puberty symptoms: Symptoms related to puberty in adolescence.
  • Radiation sickness: Illness from radiation exposure or cancer radiotherapy.
  • Recurring herpes-like penile ulcers: formation of vesicles similar to the presentation in herpes
  • Recurring prostate blockage like symptoms: conditions which cause symptoms similar to that when there is a blockage to prostate secretions
  • Recurring prostate pain symptoms: conditions which cause recurring pain similar to that of pain due to a prostatic pathology
  • Recurring prostate symptoms: symptoms related to the prostate includes painful micturition, hestiatancy and frequency of micturition
  • Recurring prostate-related urinary dribbling: weak urinary stream
  • Recurring 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
  • Recurring prostate-related weak urinary stream: weak urinary stream
  • Reduced menstrual flow: A reduced amount of blood loss during female menstruation
  • Reduced sperm count: A reduction in the normal sperm count of a males semen
  • Refractory Celiac Disease: Refractory Celiac Disease is celiac disease that fails to respond to treatment which involves a gluten-free diet. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition is quite uncommon and often the resulting poor absorption of nutrients from the intestines leads to a poor prognosis.
  • Renpenning syndrome: A very rare genetic disorder that affects males and is characterized mainly by mental retardation and facial anomalies.
  • Renpenning syndrome 1: A very rare genetic disorder that affects males and is characterized mainly by mental retardation and facial anomalies.
  • Reproductive conditions: Medical conditions of the reproductive system in men or women.
  • Reproductive toxicity -- Chlordecone (Kepone): Chlordecone (Kepone) is a suspected reproductive toxicant and exposure to it has the potential to negatively affect the human reproductive system. Chlordecone (Kepone) is used as an insecticide. The severity and nature of the adverse effect is variable and can be influenced by factors such as sex, level of exposure and individual sensitivity to the chemical. Effects on the female reproductive systems can include such things as menstrual problems, altered sexual behavior, infertility, altered puberty onset, altered length of pregnancy, lactation problems, altered menopause onset and pregnancy outcome. Effects on the male reproductive system can include such things as altered sexual behavior, altered fertility and problems with sperm shape or count.
  • Resistance to LH (luteinizing hormone): A genetic abnormality where the body is unable to respond to luteinizing hormone which affects ovarian and testicular function.
  • Retinitis pigmentosa, deafness, mental retardation, hypogonadism: A rare genetic disorder characterized by mental retardation, reduced hormone production by the testes or ovaries, deafness and vision problems.
  • Retinohepatoendocrinologic syndrome: A rare inherited disorder characterized mainly by eye, liver and endocrine function abnormalities.
  • Retinopathy pigmentary -- intellectual deficit: A rare syndrome characterized by eye disease and mental retardation.
  • Retinopathy pigmentary mental retardation: A rare genetic condition characterized by degeneration of retinal pigments, cataracts, small head and mental retardation.
  • Retinopathy, pigmentary and mental retardation: A rare syndrome characterized by eye disease and mental retardation.
  • Retrograde Ejaculation: Ejaculation that is delayed after an orgasm or does not appear to occur at all.
  • Rokitansky-Kuster-Hauser syndrome: A rare condition characterized by absence of the vagina and uterine abnormalities.
  • Round-head spermatozoa syndrome: A condition where the sperm are abnormally round-headed. The level of fertility impairment depends on how prevalent the abnormal sperm are.
  • Rud Syndrome: A condition characterized by ichthyosis, epilepsy, short stature, hypogonadism and severe mental retardation.
  • Ruvalcaba Churesigaew Myhre syndrome: A very rare syndrome characterized by early-onset senility, hypogonadism, hardening of blood vessels and thinning of the skin.
  • Ruvalcaba-Churesigaew-Myhre syndrom: A very rare syndrome characterized by early-onset senility, hypogonadism, hardening of blood vessels and thinning of the skin.
  • SIBIDS syndrome: A rare disorder characterized mainly by sulfur-deficient brittle hair as well as osteosclerosis.
  • Salti-Salem syndrome: A very rare syndrome characterized by partial alopecia and lack of secondary sex hormone production.
  • Say-Barber-Miller syndrome: A very rare syndrome characterized mainly by immune system problems and a small head.
  • Schaap-Taylor-Baraitser syndrome: A very rare syndrome characterized mainly by deafness, cataracts and a deficiency of sex hormone production.
  • Schafer syndrome: A disorder characterized mainly by thickened skin on the palms and soles, white patches in mouth, mental and growth retardation and hair, nail and eye abnormalities.
  • Scholte syndrome: A very rare syndrome characterized mainly by premature balding, dislocated kneecap, hypogonadism and small hands and feet.
  • Scrotal Ulcer: Shallow, painful sore on the skin of the scrotum.
  • Scrotal mass: A mass that is located in the scrotum of the male
  • Scrotal pain in children: Scrotal pain in children is discomfort of a boy's scrotum.
  • Scrotal rash: Change in the skin of the scrotum which affects its colour, appearance or texture.
  • Scrotal redness: Usually occurs due to inflammation or trauma to the groin area.
  • Scrotal swelling: it can occur at any age and may or maynot be associated with pain
  • Scrotal swelling in children: Scrotal swelling in children refers to a boy's scrotum that is enlarged or puffy.
  • Scrotum bleeding: Usually occurs due to injury to the scrotum.
  • Scrotum blister: Raised, small water filled lesions less than 0.5mm in diameter seen on the skin of the scrotum.
  • Scrotum bruise: Usually occurs due to trauma to the groin area.
  • Scrotum burning sensation: Abnormal burning sensation felt in the scrotal area.
  • Scrotum infection: Inflammation the groin area.
  • Scrotum inflammation: Inflammatory reaction of the groin area.
  • Scrotum itch: Unpleasant itchy sensation felt in the scrotal area.
  • Scrotum numb: Abnormal sensation of numbness felt in the scrotal area.
  • Scrotum rash: A rash that is present on the scrotum.
  • Scrotum sensitive: Raised responsiveness of the muscle of the groin to stimulus
  • Scrotum swelling: The occurrence of swelling located in the scrotum
  • Scrotum tingling: Abnormal sensations felt in the scrotal area.

Conditions listing medical symptoms: Fertility symptoms:

The following list of conditions have 'Fertility symptoms' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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Conditions listing medical complications: Fertility symptoms:

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

 

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