Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 
Symptoms » Head symptoms » Glossary
 

Glossary for Head symptoms

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

  • 10q Partial Trisomy: A very rare genetic disorder characterized by the duplication of genetic material from the long arm (q) of chromosome 10 - the genetic material occurs three times in body cells instead of the normal two. The type and severity of symptoms may vary considerably depending on the exact location and size of the duplicated genetic material.
  • 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.
  • 14q+ syndrome: A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities.
  • 14qter deletion Syndrome: A very rare genetic condition where a portion at the end of the long arm (q) of chromosome 14 is missing.
  • 18p minus syndrome: A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material that is missing.
  • 1q deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • 1q proximal deletion: A rare chromosomal disorder where the proximal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities.
  • 1q terminal deletion: A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities.
  • 2-Hydroxyglutaricaciduria: A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than others.
  • 2-Methylbutyric Aciduria: A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbutyryl-coenzyme A dehydrogenase) needed to convert the amino acid isoleucine into energy. 2-methylbutyrylglycine levels build up in the body and may cause damage. Symptoms vary according to the degree of enzyme deficiency - can range from asymptomatic to life-threatening.
  • 2-methylbutyryl-coenzyme A dehydrogenase deficiency: A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbutyryl-coenzyme A dehydrogenase) needed to convert the amino acid isoleucine into energy. 2-methylbutyrylglycine levels build up in the body and may cause damage. Symptoms vary according to the degree of enzyme deficiency - can range from asymptomatic to life-threatening.
  • 22q11.2 deletion syndrome: A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans.
  • 2p21 deletion syndrome: This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial appearance.
  • 2q deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • 2q22-q24 deletion: A rare chromosomal disorder where part of the long arm (q22-q24) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • 3 alpha methylglutaconicaciduria, type 3: A rare genetic condition where a gene mutation prevents the production of certain protein which leads to a build-up of an acid (3-methylglutaconic acid) which can have a negative impact on the body. The condition is characterized mainly by damage to the optic nerve.
  • 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay.
  • 3-Hydroxyisobutyric aciduria: A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems.
  • 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.
  • 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency: A metabolic disorder involving an enzyme deficiency which causes symptoms such as degeneration of the nervous system. The other features of the disorder are somewhat variable.
  • 3-methylglutaconic aciduria, type 1: A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine.
  • 3-methylglutaconic aciduria, type 4: A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid. Type 4 is characterized by symptoms which overlap type 1 and 3.
  • 3-methylglutaconic aciduria, type V: A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid.
  • 3?-hydroxysteroid dehydrogenase deficiency: A ver rare form of congenital adrenal hyperplasia involving a deficiency of 3?-hydroxysteroid dehydrogenase which results in reduced production of adrenal steroids (mineralocorticoids, sex steroids and glucocorticoids). The disorder can occur in classical, non-salt wasting and late-onset varieties.
  • 3C syndrome: A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name.
  • 3q deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 3 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: A very rare metabolic disorder where a deficiency of a particular enzyme results in the urinary excretion of a chemical called hawkinsin. Symptoms start once the infant is weaned off breast milk.
  • 4-hydroxyphenylacetic aciduria: A urinary abnormality usually caused by the deficiency of a particular enzyme (4-hydroxyphenylpyruvic acid oxidase). The urine contains excess 4-hydroxyphenylacetic acid.
  • 46,XX Gonadal dysgenesis epibulbar dermoid: A rare disorder characterized by gonad abnormalities and an eye disorder called epibulbar dermoid.
  • 46,XX chromosome 7 deletion p13: A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities.
  • 46,XX chromosome 7 deletion p13-p21: A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities.
  • 46,XY chromosome 7 deletion p13-p21: A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities.
  • 46,XY chromosome 7 deletion p14-p14: A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities.
  • 47 XYY syndrome: A genetic condition where males have an extra Y chromosome in each of their cells. Normally male cells have one X and one Y chromosome. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomatic.
  • 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.
  • 49,XXXXX syndrome: A rare chromosomal disorder that affects only females and involves body cells having five copies of the X chromosome instead of the normal two.
  • 49,XXXXY syndrome: A rare sex chromosome abnormality where there are three extra copies of the X chromosome.
  • 4p16.3 deletion: A rare genetic disorder where a portion of chromosome 4 is deleted at a location called 16.3. The condition is characterized by malformations in most parts of the body as the deletion affects growth and development of the fetus.
  • 6-pyruvoyl-tetrahydropterin synthase deficiency: A rare genetic disorder where insufficient levels of tetrahydropterin leads to a build up of phenylalanine in the blood which can cause toxic side effects such as nerve damage or even brain damage. The condition does not usually cause any significant symptoms.
  • 7p2 Monosomy Syndrome: A rare chromosomal disorder where there is one copy of the end 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 deleted.
  • 7th cranial nerve palsy: 7th cranial nerve palsy, also called Bell's palsy, is a paralysis of the facial muscles on one side of the face due to unknown causes that affect the facial nerve.
  • 8p-Syndrome, partial: A rare chromosomal disorder where there is one copy of part of the short arm (p) of chromosome 8 rather than the normal two. The type and severity of symptoms is determined by the location and size of the genetic material deleted.
  • A ?-protein amyloidosis: Amyloidosis is a rare group of metabolic disorders where a protein called amyloid accumulates in body organs and tissues where it can cause damage. This particular form involves deposits of ?-proteins in the nerves resulting in Alzheimer's disease or around brain blood vessels which can cause strokes or brain bleeds.
  • ABCD syndrome: A rare inherited condition characterized by albinism, deafness, a black lock of hair and intestinal abnormalities.
  • ACAD8 deficiency: An extremely rare metabolic disorder where the body is unable to metabolize certain proteins properly. More specifically, an insufficient level of the enzyme (isobutyryl-coenzyme A dehydrogenase) needed to metabolize the amino acid valine. The onset and severity of symptoms is variable.
  • ACAD9 deficiency: A metabolic disorder involving a deficiency of an enzyme (acyl-CoA dehydrogenase-9). The symptoms are variable and are usually triggered by a viral infection or ingestion of aspirin which can trigger a Reye-like episode which can cause death.
  • ACPS III: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • AChR deficiency and short channel open time: Extremely rare condition characterized by respiratory insufficiency from birth, facial dysplasia and paralysis of eye muscles.
  • ADANE: A potentially fatal inherited neurological disease involving brain lesions. Symptoms tend to occur during childhood after an illness involving a fever. The disease is similar to Leigh syndrome but the course is acute rather than chronic.
  • ADHD-like symptoms: is a neurodevelopmental behavioural disorder affecting 3-5% of the population characterised by 3 main components: hyperactivity, impulsivity and inattention. Some conditions which cause similar symptoms include
  • ADHD-like symptoms in adults: is a neurodevelopmental behavioural disorder affecting 3-5% of the population characterised by 3 main components: hyperactivity, impulsivity and inattention. Some conditions which cause similar symptoms include
  • ADHD-like symptoms in children: is a neurodevelopmental behavioural disorder affecting 3-5% of the population characterised by 3 main components: hyperactivity, impulsivity and inattention. Some conditions which cause similar symptoms include
  • ADP platelet receptor P2Y12, deficiency of: Deficiency of a compound (P2Y12) involved in the blood clotting process which results in bleeding problems.
  • ADULT syndrome: A rare syndrome characterized by nail abnormalities, abnormal teeth development, tear duct obstruction, pigmentation anomalies and hand and foot abnormalities.
  • AIDS: A term given to HIV patients who have a low CD4 count (below 200) which means that they have low levels of a type of immune cell called T-cells. AIDS patients tend to develop opportunistic infections and cancers. Opportunistic infections are infections that would not normally affect a person with a healthy immune system. The HIV virus is a virus that attacks the body's immune system.
  • AIDS dysmorphic syndrome: A rare syndrome involving craniofacial anomalies and developmental delay that occurs in infants infected with AIDS during the fetal stage.
  • AIDS-Related Opportunistic Infections: A term given to HIV patients who have a low CD4 count (below 200) which means that they have low levels of a type of immune cell called T-cells. AIDS patients tend to develop opportunistic infections and cancers. Opportunistic infections are infections that would not normally affect a person with a healthy immune system. The HIV virus is a virus that attacks the body's immune system.
  • AIDS-like recurring respiratory infections: conditions which cause respiratory infections as in case of AIDS
  • ARCA: A group of recessively inherited neurological disorders characterized mainly by cerebellar ataxia and usually with other additional abnormalities.
  • ARDS: Acute respiratory distress syndrome
  • AREDYLD: A rare condition characterized by abnormalities of the extremities, teeth, hair, nail and kidney as well as lipoatrophic diabetes.
  • ARTS syndrome: A rare lethal syndrome characterized by deafness, optic atrophy and ataxia.
  • ATR-X syndrome: A rare X-linked disorder that affects males and is characterized by mental retardation and alpha thalassemia.
  • Aarskog Syndrome: A rare genetic condition characterized by facial, hand, genital and growth abnormalities.
  • Aarskog-Ose-Pande syndrome: A rare disorder involving lipodystrophy mainly in the face and buttocks as well as sparse hair, retarded bone age and minor face and eye anomalies. It is considered a variant of SHORT syndrome which tends to also include increased range of joint motion and more extensive lipodystrophy.
  • Aase Smith syndrome: A rare hereditary syndrome characterized by deformities such as cleft palate, joint contractures and hypoplastic anemia.
  • Aase Syndrome: A genetic condition which results in anaemia and some skeletal and joint deformities
  • Aase-Smith I syndrome: A very rare hereditary syndrome characterized by deformities such as joint contractures, anemia, hydrocephalus and cleft palate.
  • Abdomen burning sensation: Burning sensation of the abdomen can be superficial or deep in nature.
  • Abdomen numbness: Sensation of abdominal numbness.
  • Abdomen sensitivity: Raised abdominal response to stimulus.
  • Abdomen spasm: Sudden involuntary contraction of the abdominal muscles.
  • Abdomen tingling: Prickling or stinging sensation felt in the abdomen.
  • 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)
  • Abdominal Cramps in Pregnancy: Abdominal Cramps in Pregnancy are spasms of pain felt in the region between the lowest line of the ribs and the pubic/pelvic bones.
  • Abdominal Pain in Pregnancy: Moderate to severe discomfort in the abdomen, occurring during pregnancy, which may or may not be related to pregnancy.
  • Abdominal Tenderness in Pregnancy: Abdominal Tenderness in Pregnancy is a painful sensation felt in the region between the lower border of the ribs and the pelvis.
  • Abdominal cramps: Painful muscular contractions occurring in the abdomen.
  • Abdominal cramps during pregnancy: Intermittant discomfort in the abdomen, related to abdominal muscles or internal organs, which may or may not be related to pregnancy.
  • Abdominal discomfort: The sensation of discomfort located in the abdomen
  • Abdominal muscle spasm: also known as abdominal rigidity
  • Abdominal pain: Pain in the abdominal area or stomach.
  • Abdominal pain exacerbated by exercise: Any acute or chronic pathological condition of the abdomen can be exacerbated by physical exercise or a sporting activity. Some of the abdominal conditions which can be worsened by exercise or sports include
  • Abdominal pain in adults: Abdominal pain in adults refers to abdominal discomfort that occurs in adults.
  • Abdominal pain in children: Abdominal pain in children refers to discomfort or pain in the abdomens of children.
  • Abdominal pain in mesenteric ischemia: Abdominal pain in mesenteric ischemia is a condition in which a person with mesenteric ischemia is experiencing abdominal discomfort.
  • Abdominal pain in the elderly: Abdominal pain in the elderly refers to an older adult who has abdominal discomfort.
  • Abdominal pain in the second trimester: Abdominal pain in the second trimester refers to pain, cramping, or discomfort that occurs in the abdomen during the second trimester of pregnancy.
  • Abdominal pain similar to Inflammatory bowel disease: it is a lower central abdominal pain
  • Abdominal pain that worsens with menses: also known as dysmenorrhea
  • Abdominal pain worsened by exercise: Abdominal pain in case of exercise is usually due to muscle cramps but previously present abdominal pain can be worsened in the following cases
  • Abdominal paradox: Abdominal paradox is a condition in which the abdomen will contract inward as the chest expands during inspiration.
  • Abdominal rebound tenderness: Where pain is felt on the release of applied pressure upon the abdomen.
  • Abdominal rebound tenderness in Pregnancy: Abdominal rebound tenderness in pregnancy is the feeling of pain that occurs immediately after an examiner removes the hand with which he/she has been palpating the abdomen.
  • Abdominal tenderness: Abdominal point tenderness refers to the pain you feel when pressure is applied to a specific part of the belly area
  • Abdominal wall burning sensation: Burning sensation of the abdomen can be superficial or deep in nature.
  • Abdominal wall inflammation: Inflammation of the abdominal wall or inflammation of the abdominal organs.
  • Abdominal wall itch: An irritating abdominal skin sensation due to various etiological factors.
  • Abdominal wall numbness: Sensation of abdominal numbness.
  • Abdominal wall sensitivity: Raised abdominal response to stimulus.
  • Abdominal wall spasm: Sudden involuntary contraction of the abdominal muscles.
  • Abdominal wall tingling: Prickling or stinging sensation felt in the abdomen.
  • Abductor lurch: deviation from the normal gait pattern expected for a child's age.
  • Abetalipoproteinemia: A rare genetic disorder involving fat metabolism. The disorder is also known as Bassen-Kornzweig syndrome. Signs of the disease include acanthocytosis, little or no serum beta-lipoproteins and hypocholesterolemia. In severe cases, steatorrhea, ataxia, nystagmus, motor incoordination and retinitis pigmentosa may also occur.
  • 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.
  • Ablinism I syndrome: A recessively inherited form of albinism involving the complete lack of skin, hair and eye pigments.
  • Abnormal Walk in Pregnancy: Abnormal Walk in Pregnancy is a change in the usual appearance of the way an adult woman moves when ambulating.
  • Abnormal brain biopsy: Abiopsy taken of the brain which reveals an abnormal result
  • Abnormal ears: Abnormal ears are irregular, deformed or malfunctioning ears.
  • Abnormal extensor reflex: also known as decerebrate posture
  • Abnormal eye movements: Uncontrollable eye movements are involuntary, rapid, and repetitive movement of the eyes.
  • Abnormal facies: queer looking kid or funny looking kid.
  • Abnormal flexor response: An abnormal flexor response is an abnormal reflex to stimulation.
  • Abnormal gait: An abnormal way of walking
  • Abnormal gait in children: Abnormal gait in children refers to a type of walk that is irregular or deviates from the normal, possibly indicating pathology.
  • Abnormal hair growth in children: Abnormal hair growth in children is an excessive or lack of normal amounts of hair in a child.
  • Abnormal head shape in children: Abnormal head shape in children is skull that is irregular or deviates from the normal head shape, possibly indicating pathology.
  • Abnormal involuntary movements of the eyes: involuntary spasms of the eyelid muscles.
  • Abnormal involuntary movements of the face: repetitive, spasmodic movement often involving the eyes and facial muscles.
  • Abnormal involuntary movements of the mouth: repetitive spasmodic movements of the oral muscles
  • Abnormal involuntary movements of the neck: repetitive spasmodic movements of the neck muscles.
  • Abnormal involuntary movements of the tongue: repetitive spasmodic movements of the tongue.
  • Abnormal movement during inspiration: decreased or increased movement of the chest wall during inspiration
  • Abnormal neuromuscular transmission: Neuromuscular disease is a very broad term that encompasses many diseases and ailments that either directly, via intrinsic muscle pathology, or indirectly, via nerve pathology, impair the functioning of the muscles
  • Abnormal pain: The abnormal presence of pain that one may feel
  • Abnormal peripheral neuropathy:
  • Abnormal pupillary response to light: the pupillary light reflex is the reduction of pupil size in response to light. A sluggish or slow pupillary response is known as an abnormal pupillary response to light
  • Abnormal pupillary size: pathological increase or decrease in the pupil size
  • Abnormal pupillary size in one eye: Abnormal pupillary size in one eye refers to an uncharacteristically small or large pupil in one eye.
  • Abnormal sensations: altered sensations due to involvement of the posterior column
  • Abnormal sensations as in case of diabetes mellitus: altered sensations due to involvement of the posterior column
  • Abnormal sensitivity to light: dislike of bright light
  • Abnormal sensitivity to light in both eyes: Abnormal sensitivity to light in both eyes is a condition in which the eyes are unusually sensitive to light, also called photosensitivity.
  • Abnormal sensitivity to light in one eye: Abnormal sensitivity to light in one eye is a condition in which one eye is unusually sensitive to light, also called photosensitivity.
  • Abnormal sensory nerve action potential and sensory conduction velocity: An investigation used to determine nerve function and the conduction velocity of a nerve
  • Abnormal spasm of the facial muscles: a jerk usually caused by sudden muscle contractions
  • Abnormal spasm of the facial nerve: inflammation of the peripheral nervous system. Often representing as Bell's palsy
  • Abnormal taste sensation: Abnormal taste sensation refers to an unusual or unexpected taste in the mouth.
  • Abnormal teeth shape in children: Abnormal teeth shape in children includes any type of deformity or irregularity in the dentition or teeth.
  • Abnormal thinking: Abnormal thinking is any type of thought process that is considered deviant or outside of what is expected, usual, understandable, or typical.
  • Abnormal thinking in pregnancy: Abnormal thinking in pregnancy is a deviation from the woman's usual, expected thought processes or attitude.
  • Abnormal walk: An abnormal walk is any type of gait that is irregular, unsteady, or unusual, possibly indicating pathology.
  • Abrupt loss of vision in both eyes: Abrupt loss of vision in both eyes is a serious condition in which there is sudden blindness or decreased, disrupted, or blurred vision in both eyes.
  • Abrupt loss of vision in one eye: Abrupt loss of vision in one eye is a serious condition in which there is sudden blindness or decreased, disrupted, or blurred vision in one eye.
  • Abruzzo Erickson syndrome: A genetic disorder characterized by a combination of features including cleft palate, coloboma and deafness.
  • Abscess: This is an area of puss collected in a cavity which is constituted by necrotised tissue
  • Abscessed teeth: an abscessed tooth is a painful infection at the root of a tooth or between the gum and a tooth
  • Absence of both eyebrows: Absence of both eyebrows is a lack of eyebrows.
  • Absence of doll's eye sign: Reflex movement of the eyes such that the eyes lower as the head is raised, indicating functional integrity of the nerve pathways involved in eye movement
  • Absence of pulmonary artery: The absence of a pulmonary artery at birth.
  • Absence of septum pellucidum and septo-optic dysplasia: A rare birth defect where a thin membrane in the middle of the brain is missing. This brain abnormality is never present on it's own but is a characteristic of septo-optic dysplasia where the patient also has optic disk abnormalities and pituitary deficiencies.
  • Absence of septum pellucidum with porencephalia syndrome: A rare syndrome present at birth and characterized by the absence of the thin membrane in the middle of the brain (septum pellucidum) as well as abnormal cavities in the brain (porencephaly). The syndrome also involves other structural brain abnormalities.
  • Absence of thirst in children: Absence of thirst in children is a condition in which a child is not thirsty.
  • Absence seizure: An epileptic seizure involving momentary loss of consciousness.
  • Absent abdominal musculature with microphthalmia and joint laxity: A rare disorder characterized mainly by small eyes, loose joints, a lack of abdominal muscles and facial anomalies.
  • Absent abdominal reflexes: the abdominal reflex includes contraction of abdominal muscles in the quadrant of the abdomen that is stimulated by scraping the skin tangential to or toward the umbilicus. This contraction can often be seen as a brisk motion of the umbilicus toward the quadrant that is stimulated, it is absent in ceratin conditions
  • Absent alpha 1 band: An absence of alpha-1-antitrypsin the the body
  • Absent corneal reflex: Loss of blinking when the edge of the cornea is touched.
  • Absent corneal reflex in one eye: Absent corneal reflex in one eye is the lack of a blink reflex in one eye.
  • Absent corpus callosum -- cataract -- immunodeficiency: A rare syndrome characterized by immunodeficiency, cleft lip or palate, cataract, reduced pigmentation and brain abnormalities.
  • Absent eyebrows: Absent eyebrows is a condition in which the eyebrows are not present.
  • Absent patellae -- scrotal hypoplasia -- renal anomalies -- facial dysmorphism -- mental retardation: A rare syndrome characterized by absent kneecaps, underdeveloped scrotum, kidney anomalies, unusual facial appearance and mental retardation.
  • Absidia species poisoning: Absidia species is a type of fungus found in plant debris but is also common in the environment. 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.
  • Absolute Glaucoma: The final stage of blindness in glaucoma in which a glaucoma-induced increase in intraocular pressure results in permanent vision loss.
  • Acalvaria: A rare congenital condition where the skull cap is missing but the rest of the face and base of the skull is normal. The skin of the scalp simply covers the brain with no protective skull bone under it.
  • Acanthamoeba: Several conditions from infection with ameba.
  • Acanthamoeba infection: Infection with a microscopic, free-living ameba that is readily found in the environment - soil, air and water. Most people exposed to the ameba will not become infected but when infections do occur, they tend to affect the eyes, central nervous system or can cause widespread infection throughout the body.
  • Acanthamoeba infection of the central nervous system: Infection by an amoebic organism called Acanthamoeba. Infection usually occurs when the amoeba enters through a break in the skin or through the nose. Infection can be localized or systemic where it can involve the central nervous system and cause potentially fatal meningoencephalitis. Infection of the eye can occur by cleaning contact lenses in contaminated water.
  • Acanthamoeba infection of the eye: Infection by an amoebic organism called Acanthamoeba. Infection usually occurs when the amoeba enters through a break in the skin or through the nose. Infection can be localized or systemic where it can involve the central nervous system and cause potentially fatal meningoencephalitis. Infection of the eye can occur by cleaning contact lenses in contaminated water.
  • Acanthamoeba keratitis: Infection of the eye with a microscopic, free-living ameba (Acanthamoeba) that is readily found in the environment - soil, air and water. Infection most often occurs through exposure to contaminated water while wearing contact lenses e.g. swimming or showering in infected waters.
  • Acanthocheilonemiasis: A rare tropical infection caused by a particular threadworm usually found in Africa. It may cause skin rashes, muscle and joint pains, neurologic disorders and skin lumps. The cerebrospinal fluid may also contain the larvae.
  • Acanthocytosis: A rare disorder where most of the red blood cells are abnormal with spiny projections due to lipid abnormalities. The blood abnormality is seen in conditions such as abetalipoproteinemia, severe liver disease and severe malnutrition. Symptoms and prognosis depend on the underlying disorder.
  • Acatalasemia: A rare genetic deficiency where little or no catalase is produced.
  • Accelerated hypertension: Accelerated hypertension is a condition characterized by a rapid increase in blood pressure. The condition is a medical emergency which can cause organ damage if not treated promptly.
  • Accelerated silicosis: An occupation lung disease caused by breathing in silica dust over a long period of time. The lung damage becomes symptomatic and affects breathing and often causes weight loss as well.
  • Accessory bone pain in children: Accessory bone pain in children is any discomfort or pain in the accessory bones in children.
  • Accessory muscle use: The use of accessory muscles
  • Accidental Eye Injury: The accidental injury to an eye
  • Accutane -- Teratogenic Agent: There is strong evidence to indicate that the use of Accutane during pregnancy may cause 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.
  • Aceruloplasminemia: A rare genetic disorder characterized by a lack of the protein ceruloplasmin in the blood resulting in a buildup of iron in the liver, brain and pancreas. This in turn causes diabetes and degeneration of the neural system causing tremors and walking abnormalities.
  • Acetaminophen -- Teratogenic Agent: There is strong evidence to indicate that exposure to Acetaminophen 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.
  • Achalasia: A rare condition where the patients muscles, such as the cardiac sphincter of the stomach, are unable to relax.
  • Achalasia -- Addisonianism -- Alacrimia syndrome: A rare inherited disorder characterized mainly by achalasia, alacrimia (absent tears) and Addison's disease. Addison's disease involves adrenal insufficiency due to a resistance to adrenocorticotropic hormone. Only about 70 cases reported worldwide.
  • Achalasia -- addisonianism -- alacrima syndrome: A rare inherited disorder characterized mainly by achalasia, alacrimia (absent tears) and Addison's disease. Addison's disease involves adrenal insufficiency due to a resistance to adrenocorticotropic hormone. Only about 70 cases reported worldwide.
  • Achalasia -- adrenal -- alacrima syndrome: A familial disorder characterized by adrenal gland-related hormonal problems, swallowing difficulty (achalasia) and a lack of tears (alacrima). Neurological impairment and motor and sensory neuropathy is progressive. The adrenal glands in patients are resistant to the ACTH hormone and hence fails to operate normally.
  • Achalasia microcephaly: A very rare syndrome characterized primarily by a small head and achalasia which involves esophageal problems such as enlargement.
  • Achalasia, familial esophageal: A rare familial disorder where the esophagus lacks the normal peristaltic motions that help food move through the digestive system.
  • Achalasia, primary: A rare motor disorder of the esophagus characterized by inability of the lower esophageal sphincter and esophageal muscle to relax as well as dilation of the esophagus. The disorder is not associated with any other disease or disorder.
  • Achard syndrome: An inherited connective tissue disorder characterized primarily by a short head, long, slender bones, recessed lower jaw and loose hand and foot joints.
  • Achard-Thiers Syndrome: A rare hormonal disorder that occurs in diabetic postmenopausal women where body hair grows in a masculine manner. Hormonal therapy is used to correct the endocrine imbalance.
  • Aches: General body aches or muscle aches
  • Aches in pregnancy: Aches in pregnancy are physical areas of discomfort felt in any part of the body, but usually confined to the torso, including the pelvis and ribs. Aching legs are also common.
  • Achilles tendon burning sensation: burning sensation of the Achilles tendon usually due to systemic disorders.
  • Achilles tendon bursitis due to running: It is estimated that Achilles tendonitis accounts for around 11% of all running injuries. The Achilles tendon is the large tendon at the back of the ankle. The achilles tendon can become inflamed through overuse as well as a number of contributory factors. The Achilles tendon has a poor blood supply which is why it is slow to heal.
  • Achilles tendon numb: Abnormal sensations felt in the Achilles tendon.
  • Achilles tendon pain: Achilles tendon also known as the calcaneal tendon is the tendon of the posterior part of the leg.
  • Achilles tendon sensitive: Increased responsiveness to stimulation.
  • Achilles tendon spasm: Sudden involuntary contraction of the Achilles tendon.
  • Achilles tendon stiff: tendon stiffness due to physical trauma or abnormal muscle contraction.
  • Achilles tendon tingling: Prickling or stinging sensation felt in the Achilles tendon.
  • Aching eyes: A sensation of aching located in the eyes
  • Aching joints: A sensation of aching located in the joints
  • Aching muscles in children: Aching muscles in children is a condition in which a child's muscles ache.
  • Aching muscles of both arms: Aching muscles of both arms is an aching of the muscles of both arms.
  • Aching pain: severe pain in the body
  • Achlorhydria: Condition where there is no hydrochloric acid in the gastric juice
  • Achondrogenesis: A type of dwarfism where the main limbs are short and the head and trunk are hydropic (contain an accumulation of clear fluid).
  • Achondrogenesis type 1A and 1B: A rare lethal genetic disorder characterized by a low nasal bridge, very short limbs and incomplete bone formation of lower spine.
  • Achondrogenesis type 1B: A rare lethal genetic disorder characterized by a low nasal bridge, very short limbs and incomplete bone formation of lower spine.
  • Achondrogenesis type 2: A rare genetic disorder characterized by very small stature, abnormal bone formation and early death.
  • Achondrogenesis, Langer-Saldino Type: A rare genetic disorder characterized by very small stature, abnormal bone formation and early death.
  • Achondrogenesis, type 4: A rare genetic disorder characterized by very small stature, abnormal bone formation and early death. It has been designated as a mild form of Langer-Saldino achondrogenesis.
  • Achondroplasia: A rare disease characterized by abnormal bone growth which results in short stature with short arms and legs, large head and characteristic facial features.
  • Achrestic anemia: Achrestic anemia is a form of anemia similar to that caused by Vitamin B12 deficiency but it doesn't respond to treatment with Vitamin B12. The condition tends to progress slowly and can result in death if not treated. There are a variety of possible causes.
  • Achromatopsia: Patients who have achromatopsia (sometimes called achromatopia) do not have normal "cone vision.". Although the term may refer to acquired disorders such as color agnosia and cerebral achromatopsia, it typically refers to an autosomal recessive congenital color vision disorder, the inability to perceive color AND to achieve satisfactory visual acuity at high light levels (typically exterior daylight).
  • Achromatopsia 2: A rare form of colorblindness involving atypical rod monochromatism which and causing pendular nystagmus and photophobia.
  • Achromatopsia 3: A rare form of colorblindness which also involves myopia.
  • Achromatopsia incomplete, X-linked: An inherited form of blue color blindness.
  • Achromatopsia type 2: A rare form of colorblindness involving atypical rod monochromatism which and causing pendular nystagmus and photophobia.
  • Achromatopsia with Myopia: A rare form of colorblindness which also involves myopia.
  • Acid Reflux in pregnancy: Acid Reflux in pregnancy is the movement of the acid contents of the stomach through the gastro-oesophageal sphincter up into the oesophagus, causing a burning, pain or discomfort in the chest, commonly known as heartburn.
  • Acid reflux: Condition which occurs when the acid reflux into the oesophagus exceeds the normal limit
  • Acid reflux / heartburn:
  • Acid reflux into mouth: acid reflux related disorders
  • Acid regurgitation: The regurgitation of stomach contents
  • Acid-Base Imbalance: A disruption to the normal acid-base equilibrium in the body. There are four main groups of disorder involving an acid-base imbalance: respiratory acidosis or alkalosis and metabolic acidosis or alkalosis. Obviously the severity of symptoms is determined by the degree of imbalance.
  • Acidemia, isovaleric: A rare genetic condition where the body can't process proteins adequately. More specifically, there are insufficient levels of the enzyme needed to break down an amino acid called leucine. This results in a build up of isovaleric acid which can harm the brain and nervous system. Some people suffer severe symptoms from birth and others suffer milder symptoms that come and go and are affected by such things as infections or consumption of high protein food.
  • Acidemia, methylmalonic: An inborn error of metabolism where amino acids in the body aren't metabolized properly resulting in high levels of the acid throughout the body.
  • Acidemia, propionic: An inherited genetic disorder where the body is incapable of processing some proteins and fats resulting in the accumulation of certain substances in the body which causes the symptoms of the condition. The condition can be life threatening.
  • Acidic dry cell batteries inhalation poisoning: Acidic dry cell batteries contain toxic chemicals which can cause symptoms if inhaled. The smoke emitted from burning batteries can also cause poisoning symptoms if sufficient quantities are inhaled. The type and severity of symptoms varies depending on the amount of chemical involved.
  • Acidic tastes: Acidic or metallic taste in mouth
  • Acitretin- Teratogenic Agent: Reports indicate that the use of Acitretin during pregnancy may cause various harmful effects on the fetus. The likelihood and severity of symptoms may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at. Acitretin should not be taken by women who are pregnant or planning on becoming pregnant.
  • Ackee Fruit Food poisoning: Unripe ackee fruit contains a chemical called hypoglycin A and B which affect the central nervous system and fatty acid oxidation. Eating the unripe fruit can cause symptoms can occur in as little as two hours but is generally 6 to 48 hours. The ackee fruit is found mainly in Jamaica, West Africa, Central America, Sought Florida, southern California and Hawaii.
  • Ackerman syndrome: An extremely rare condition characterized primarily by glaucoma, upper lip deformity and abnormal tooth roots.
  • Acne-like cheek symptoms: acne is a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acne-like facial skin symptoms: reddish raised elevated patches on the face.It is a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acne-like facial symptoms: reddish raised elevated patches on the face
  • Acne-like forehead symptoms: reddish raised elevated lesions on the forehaed
  • Acne-like nose symptoms: reddish raised elevated lesions on the nose
  • Acoustic Neurinoma: A benign tumor of the 8th cranial nerve which lies in the tube connecting the inner ear to the brain.
  • Acoustic neuroma: A rare benign tumor that forms in the hearing canal. Can cause tinnitus, progressive hearing loss, headaches, facial numbness, papilledema, dizziness and an unsteady walk. Speaking and swallowing difficulty can occur in advanced stages. Also called acoustic neurilemoma, acoustic neurinoma and acoustic neurofibroma.
  • Acquired Aplastic Anemia: A rare disorder involving severe failure of the bone marrow to produce new blood cells. Acquired aplastic anemia means that the condition was not present at birth but developed during the persons lifetime. The condition may be caused by such things as autoimmune reactions, radiation and certain drugs, chemicals or viral infections.
  • Acquired agranulocytosis: A blood disorder characterized by low levels of white blood cells (granular leukocytes) in the circulating blood. The condition is usually caused by certain drugs especially chemotherapy drugs.
  • Acquired angioedema: A rare disorder characterized by recurring episodes of swelling of parts of the skin or mucous membranes. Sometimes internal organs may be involved. The disorder occurs in patients with lymphoproliferative or autoimmune disorders which result in the dysfunction of a complex blood protein called C1 inhibitor.
  • Acquired angioedema, type 1: A rare disorder characterized by recurring episodes of swelling of parts of the skin or mucous membranes. Sometimes internal organs may be involved. The disorder occurs in patients with lymphoproliferative disorders which affects the function of a complex blood protein called C1 inhibitor.
  • Acquired angioedema, type 2: A rare disorder characterized by recurring episodes of swelling of parts of the skin or mucous membranes. Sometimes internal organs may be involved. Type 2 is an autoimmune disorder where patients develop autoantibodies which destroy the function of C1 esterase inhibitor.
  • Acquired conductive hearing loss in children: Acquired conductive hearing loss in children is a type of hearing loss or deafness that is not present at birth and occurs in children due to an abnormality or disease of the outer or middle ear.
  • Acquired facial paralysis in children: Acquired facial paralysis in children is paralysis or the facial muscles in children that is due to a disease or cause that is not present at birth and is acquired later in life.
  • Acquired hypothyroidism: Acquired hypothyroidism is a condition where the thyroid gland makes too little or no thyroid hormone. Acquired hypothyroidism can be caused by both thyroid disease (primary hypothyroidism) and hypothalamic-pituitary disease (central hypothyroidism)
  • Acquired progressive kinky hair: An acquired hair condition involving the progressive kinking of hair. It often precedes the early stages of male pattern alopecia.
  • Acquired prothrombin deficiency: A deficiency of prothrombin (vital for blood clotting) which is acquired through other conditions such as liver disease, anticoagulant drugs or vitamin K deficiency. The severity of symptoms is determined by the degree of deficiency.
  • Acquired stridor in children: Acquired stridor in children is an abnormal sound made during breathing that is not present at birth and is acquired later in life.
  • 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.
  • Acro-reno-ocular syndrome: A disorder characterized by eye abnormalities, kidney defects and abnormalities of the arm and hand bones.
  • Acrocallosal Syndrome (Schinzel Type): A rare condition characterized by absence of portion of the brain (corpus callosum), mental deficiency, duplicated toes, mental deficiency and other abnormalities.
  • Acrocallosal syndrome: A rare genetic disorder characterized by underdeveloped or absent corpus callosum of brain, duplication of thumb or big toe and extra fingers or toes.
  • Acrocephalopolydactyly: A rare genetic condition characterized by limb abnormalities, extra digits and hydrocephalus. Other additional symptoms are variably present.
  • Acrocephalopolydactyly -- Cardiac Disease -- Ear, Skin and Lower Limb Defects: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • Acrocephalopolydactyly II: A rare genetic disorder characterized by head, hand and genital anomalies as well as mental retardation.
  • Acrocephalopolysyndactyly type III: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • Acrocephalopolysyndactyly, type 2 (ACPS 2): A rare genetic disorder characterized by premature closing of skull bones, craniofacial abnormalities, heart defects, growth retardation and other disorders.
  • Acrocephalosyndactyly: A group of inherited disorders characterized by abnormalities involving the skull, face, hands and feet. Apert, Pfeiffer and Crouzon syndrome are examples of various types of the disorder.
  • Acrocephalosyndactyly II: A rare inherited disorder characterized primarily by premature closure of skull bones, fusion of fingers and toes and eye and face abnormalities.
  • Acrocephalosyndactyly Syndrome type 5: A rare genetic disorder where some of the skull bones fuse too early which affects the size and shape of the skull and face. Thumb and toe abnormalities are also present. There are three types of Pfeiffer syndrome with varying degrees of severity.
  • Acrocephalosyndactyly type 3 (ACPS 3): A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include brachycephaly, ear deformities as well as craniofacial, finger and bone abnormalities.
  • Acrocephalosyndactyly type 5 (ACPS 5): A rare genetic disorder where some of the skull bones fuse too early which affects the size and shape of the skull and face. Thumb and toe abnormalities are also present. There are three types of Pfeiffer syndrome with varying degrees of severity.
  • Acrodermatitis Enteropathica: A rare, chronic condition that occurs in infants and involves autosomal zinc malabsorption. Signs include blisters on the skin and mucous membranes, alopecia, diarrhea and failure to thrive. The condition may be fatal if untreated.
  • Acrodynia: A disease occurring in infants or young children. Symptoms include edema, pruritis, skin rash, extremities are pink, cheeks and nose are scarlet, profuse sweating, digestive disturbance, photophobia, polyneuritis, irritability, listlessness, apathy and failure to thrive.
  • Acrodysostosis: A rare genetic disorder characterized by short hands, small nose, mental deficiency and hand and foot deformities.
  • Acrofacial dysostosis Catania form: One of a group of disorders characterized by defective limb and facial development. The Catania form is very rare.
  • Acrofacial dysostosis Preis type: One of a group of disorders characterized by defective limb and facial development. The Preis type is very rare and the range and severity of symptoms is variable.
  • Acrofacial dysostosis Rodriguez type: One of a group of disorders characterized by defective limb and facial development. The Rodriguez type is very rare and primarily involves severe limb and organ malformations.
  • Acrofacial dysostosis atypical postaxial: A rare genetic disorder characterized by absence of some fingers and toes and characteristic facial features.
  • Acrofacial dysostosis autosomal recessive: A rare inherited disorder characterized mainly by facial, hand and foot anomalies. The disorder resembles Nager syndrome.
  • Acrofacial dysostosis postaxial, atypical: A rare disorder characterized by an unusual facial appearance, short stature and hand and foot bone anomalies. The disorder may be related to the fact that the infants were born to mothers with diabetes.
  • Acrofacial dysostosis, Nager type: A rare genetic disorder characterized by underdeveloped thumbs, forearm and cheekbones as well as ear defects.
  • Acrofacial dysostosis, Palagonia type: One of a group of disorders characterized by defective limb and facial development. The Palagonia type is very rare and the symptoms are relatively mild.
  • Acrofacial dysostosis, Weyers type: A rare disorder characterized by facial abnormalities and extra digits, nail abnormalities and short limbs.
  • Acrofrontofacionasal dysostosis syndrome: A very rare syndrome characterized by abnormalities of the bones of the skeleton as well as mental retardation. Various facial, eye and urogenital anomalies are also present.
  • Acrogeria (Gottron Type): An extremely rare, mild form of progeria.
  • Acromegaloid changes, cutis verticis gyrata and corneal leukoma: A rare disorder characterized by acromegaly (enlarged extremeties) , furrowed skin on scalp and face and corneal leukomas.
  • Acromegaloid facial appearance syndrome: A very rare genetic disorder characterized by thick lips and gums, thick upper eyelids, large hands and occasionally mental deficiency.
  • Acromegaloid facies -- hypertrichosis: A very rare genetic disorder characterized by thick lips and gums, thick upper eyelids, large hands and occasionally mental deficiency.
  • Acromegaloid hypertrichosis syndrome: A rare genetic condition characterized by excess body hair and a coarse face. The severity of the condition is variable.
  • Acromegaloid, Cutis Verticis Gyrata, Corneal Leukoma Syndrome: A rare condition characterized by the association of acromegaly, cutis verticis gyrate and corneal leukoma.
  • Acromegaly: An abnormal enlargement of the limbs due to increased secretion of growth hormone after the cessation of puberty
  • Acromegaly due to growth hormone-secreting pituitary adenoma: Pituitary adenomas are benign monoclonal neoplasms of the anterior pituitary gland, accounting for approximately 15% of intracranial tumors.
  • Acromelic frontonasal dysplasia: A very rare genetic malformation syndrome characterized by developmental abnormalities of the face and brain.
  • Acromesomelic dysplasia: A rare genetic progressive skeletal disorder characterized by short limbs, a large head and lower thoracic kyphosis.
  • Acromesomelic dysplasia, Maroteaux type: A rare genetic syndrome characterized by various developmental abnormalities of the skeletal bones and facial anomalies.
  • Acromicric dysplasia: A rare genetic syndrome characterized by various severe developmental abnormalities of the skeletal bones and facial anomalies.
  • Acroosteolysis dominant type: A rare inherited connective tissue disorder characterized by breakdown of bone especially in the ends of the fingers and toes.
  • Acroosteolysis neurogenic: A very rare inherited condition characterized mainly by the loss of all sensations - the lose the ability to feel pain, temperature and touch. The loss of sensation generally starts at the toes and fingers and spreads up the limbs and the trunk may also be involved in some cases.
  • Acrorenal mandibular syndrome: A very rare condition characterized by a split hand or foot deformity, kidney abnormalities and underdeveloped lower jaw.
  • Acrosphenosyndactylia: A rare condition characterized by abnormalities in the appearance of the face and head as well as finger and toe abnormalities. The bones of the skull fuse together too early which prevents it from growing normally. Various toes and fingers may be fused together.
  • Actinic cheilitis: Degeneration of the lip due to sun damage. The condition is considered precancerous.
  • Actinic prurigo: An inherited tendency to develop an itchy, bumpy rash on exposure to the sun. Generally only the face and lips are affected. Symptoms tend to occur seasonally.
  • Actinomycetales infection: A bacterial infection from the order of Actinobacteria. The range of symptoms is variable depending on which bacteria from the order is involved.
  • Actinomycosis: A chronic infection usually caused by an organism normally found in human bowels and mouths. The disease usually affects the face and neck and results in deep, lumpy abscesses that emit a grainy pus through multiple sinuses.
  • Acutane embryopathy: A rare disorder caused by fetal exposure to retinoids and resulting in mental and physical birth defects.
  • Acute (or transient) urinary incontinence: Acute (or Transient) Incontinence is caused by a new or recent medical problem that can be treated.
  • Acute AIDS-like recurring respiratory infections: conditions which causes respiratory infections as in case of AIDS
  • Acute Alzheimers-like concentration difficulty: maybe to due to various causative agents
  • Acute Alzheimers-like confusion symptoms: unalterable confusion state
  • Acute Alzheimers-like memory loss: also known as dementia
  • Acute Alzheimers-like symptoms: symptoms such as dementia
  • Acute Angle Closure Glaucoma: Primary angle closure is defined as an occludable drainage angle and features indicating that trabecular obstruction by the peripheral iris has occurred (ie, peripheral anterior synechiae, increased IOP, lens opacities, excessive trabecular pigmentation deposits).
  • Acute Bokhoror: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute COPD-like cough symptoms: usually comprises of cough with sputum
  • Acute COPD-like symptoms: symptoms such as dyspnea, cough with sputum , wheeze etc
  • Acute Chemical poisoning -- Varnish makers' and painters' Naptha: Varnish makers' and painters' Naptha is an ingredient used in certain pesticides. Exposure to the chemical can cause a range of symptoms depending on the level and route of exposure. Exposure can occur through inhalation, ingestion, the skin or eyes. Acute exposure involves a exposure over a short period of time whereas chronic exposure occurs over a longer period of time.
  • Acute Disseminated Encephalomyelitis: A type of encephalitis that usually follows an acute viral infection and involves an immune attack on myelin tissue which is part of the nervous system. Initial symptoms include fever, headache, vomiting and drowsiness followed by seizures, coma and paralysis. Often results in permanent neurological disorders.
  • Acute Dyspnoea: The acute sensation of shortness of breath
  • Acute Dyspnoea in pregnancy: acute dyspnoea in pregnancy is the sudden onset of a feeling of difficulty breathing occurring in a pregnant woman.
  • Acute Interstitial Pneumonia: A relatively uncommon form of pneumonia that has no apparent cause. Symptoms tend to develop over a period of six months to one and a half years.
  • Acute Pesticide poisoning -- Ureas: Urea is a class of active ingredients used in certain defoliants, herbicides, insecticides and rodenticides. Exposure to the chemical can cause a range of symptoms depending on the level and route of exposure. Exposure can occur through inhalation, ingestion, the skin or eyes. Acute exposure involves a exposure over a short period of time whereas chronic exposure occurs over a longer period of time.
  • Acute Pesticide poisoning -- xylene: Xylene is an ingredient used in certain insecticides. Exposure to the chemical can cause a range of symptoms depending on the level and route of exposure. Exposure can occur through inhalation, ingestion, the skin or eyes. Acute exposure involves a exposure over a short period of time whereas chronic exposure occurs over a longer period of time.
  • Acute Posterior Multifocal Placoid Pigment Epitheliopathy: A acute acquired condition which is an inflammatory one affecting the retina of healthy young adults
  • Acute Silicosis: An occupation lung disease caused by breathing in high levels of silica dust.
  • Acute Tracheitis: Tracheitis is a bacterial infection of the trachea and is capable of producing airway obstruction
  • Acute VE: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Viliuisk Encephalitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Viliuisk Encephalomyelitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Vilyuisk Encephalitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Vilyuisk Encephalomyelitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Vision Changes in Both Eyes (with pain or inflammation): Vision changes occurring in both eyes, of sudden onset or over a short term period of hours to days with associated symptoms of pain and/or inflammation.
  • Acute Vision Changes in Both Eyes (without pain or inflammation): Vision changes occurring in both eyes, of sudden onset or over a short term period of hours to days without symptoms of pain or inflammation.
  • Acute Vision Changes in One Eye (Without pain or inflammation): Vision changes occurring in one eye only, of sudden onset or over a short term period of hours to days without symptoms of pain or inflammation.
  • Acute abdominal pain: Sudden onset pain occurring within the abdomen.
  • Acute abdominal pain in pregnancy: Acute abdominal pain in pregnancy is the sudden onset of abdominal pain in the pregnant woman.
  • Acute acid reflux into mouth: acid reflux related disorders
  • Acute acid reflux into mouth during pregnancy: Reflux-like vomiting in pregnancy is the movement of the acid contents of the stomach through the gastro-oesophageal sphincter up into the oesophagus, causing a burning, pain or discomfort in the chest, commonly known as heartburn and followed by an episode of vomiting.
  • Acute acne-like cheek symptoms: acne is a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acute acne-like facial skin symptoms: reddish raised elevated patches on the face.Itis a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acute acne-like facial symptoms: reddish raised elevated patches on the face
  • Acute acne-like forehead symptoms: reddish raised elevated lesions on the forehaed
  • Acute acne-like nose symptoms: reddish raised elevated lesions on the nose
  • Acute adhd-like symptoms: is a neurodevelopmental behavioural disorder affecting 3-5% of the population characterised by 3 main components: hyperactivity, impulsivity and inattention. Some conditions which cause similar symptoms include
  • Acute adhd-like symptoms in adults: is a neurodevelopmental behavioural disorder affecting 3-5% of the population characterised by 3 main components: hyperactivity, impulsivity and inattention. Some conditions which cause similar symptoms include
  • Acute adhd-like symptoms in children: is a neurodevelopmental behavioural disorder affecting 3-5% of the population characterised by 3 main components: hyperactivity, impulsivity and inattention. Some conditions which cause similar symptoms include
  • Acute allergy-like breathing symptoms: difficulty in breathing due to allergy symptoms
  • Acute allergy-like cough: allergic cough varies with the position of the body
  • Acute allergy-like eye redness: redness of the eye maybe due to conjunctival, scleral or corneal inflammation
  • Acute allergy-like runny eyes: allergy is one of the main factors for watering of eyes
  • Acute allergy-like runny nose: allergy is one of the main factors for runny nose
  • Acute allergy-like sneezing symptoms: allergy causes runny nose, sneezing and headache
  • Acute appendicitis: Infection of the appendix
  • Acute asthma-like breathing attacks: asthma sometimes causes sudden, acute episodes of dyspnea
  • Acute asthma-like breathing difficulty: also known as dyspnea
  • Acute asthma-like symptoms: sudden severe asthma usually presents with difficulty in breathing, wheeze, cough and stridor
  • Acute asthma-like symptoms at night: also known as paroxysmal nocturnal dyspnea
  • Acute asthma-like symptoms non-responsive to treatment: some of the symptoms of asthma such as dyspnoea, wheeze and cough maybe be non-responsive to treatment
  • Acute asthma-like wheezing symptoms: wheeze is a continuous, coarse, whistling sound produced in the respiratory airways during breathing
  • Acute attack of asthma:
  • Acute blindness: An acute loss of vision
  • Acute bronchitis: Respiratory inflammation of the bronchi leading to the lungs
  • Acute chest pain: The sudden and acute onset of pain in the chest
  • Acute cholinergic dysautonomia: A rare condition characterized by the presence of abnormal red blood cells in the bone marrow and blood. The condition is characterized by anemia and generally leads to the development of acute myelogenous leukemia. The acute form has more severe symptoms than the chronic form.
  • Acute chronic bronchitis-like cough: cough with white colored sputum
  • Acute chronic bronchitis-like symptoms: symptoms of cough with sputum
  • Acute chronic headache not migraine-related: conditions which causes severe headache other than migraine
  • Acute chronic herpes-like genital pain: formation of vesicles seen commonly in a rash
  • Acute chronic joint pain: pain in the joints
  • Acute chronic kidney pain: renal related etiologies
  • Acute chronic knuckle pain: severe pain of the heads of the metacarpal bones
  • Acute chronic pain in multiple bones: occurs during physical exercise and is relieved by rest. It usually is a feature of arterial abnormality
  • Acute chronic pain symptoms: continous deep seated pain
  • Acute chronic spinal pain: diseases of the spinal cord
  • Acute chronic tailbone pain: pain due to lesions in the coccyx
  • Acute chronic vaginal pain: pathologies of the vagina
  • Acute colitis-like abdominal pain: conditions which cause pain abdomen similar to that in case of colitis
  • Acute collarbone pain: acute pain due to pathologies related to the clavicle
  • Acute concentration difficulty in adults: maybe to due to various causative agents
  • Acute concentration difficulty with headache-like symptoms: is mostly due to an organic cause
  • Acute congestive glaucoma: This is a closed angle type of glaucoma, caused by contact between the iris and trabecular meshwork, which in turn obstructs outflow of the aqueous humor from the eye.
  • Acute conjunctival inflammation: Acute conjunctival inflammation is the sudden onset of redness and irritation of the membranes that covers the white of the eyes and the inner part of the eyelids.
  • Acute cough: The noisy sudden expulsion of air from the respiratory tract
  • Acute cough in children: Acute cough in children is a sudden onset of coughing in a child.
  • Acute cranial nerve dysfunction: dysfunction of certain cranial nerves may affect the eye, pupil, optic nerve, or extraocular muscles and their nerves; thus, they can be considered cranial nerve disorders, neuro-ophthalmologic disorders, or both
  • Acute croup-like breathing difficulty: also known as laryngotracheobronchitis.Croup is characterized by a harsh "barking" cough and sneeze, inspiratory stridor (a high-pitched sound heard on inhalation), nausea/vomiting, and fever
  • Acute croup-like symptoms: also known as laryngotracheobronchitis. Croup is characterized by a harsh "barking" cough and sneeze, inspiratory stridor (a high-pitched sound heard on inhalation), nausea/vomiting, and fever
  • Acute cry: a brief, sharp, piercing vocal sound produced by a neonate or infant.
  • Acute diabetes-like neuropathy symptoms: also known as peripheral neuropathy is a typical presentation of diabetes but can be a presentation of other diseases too
  • Acute diabetes-like paresthesia symptoms: sensation of sudden, rapid pricking or numbness. It is also called "pins and needles sensation"
  • Acute diabetes-like retinopathy symptoms: diabetic retinopathy can cause many sudden changes in the retinal pattern such as microaneurysms, cotton-wool spots, flame-shaped hemorrhages and hard exudates
  • Acute difficulty concentrating at work: is mostly related to stress
  • Acute difficulty concentrating for long periods: concentrating difficulty which occurs only during particular periods
  • Acute dyspnea following trauma: Acute dyspnea following trauma is a condition in which a person experiences a sudden onset of difficulty breathing after an injury or accident.
  • Acute elbow pain: conditions of the elbow which can cause acute pain for a long period of time
  • Acute elemental mercury inhalation: Inhalation of elemental mercury can lead to breathing and lung symptoms of various degrees of severity depending on the level of exposure.
  • Acute emphysema-like cough symptoms: is usually associated with with white colored sputum
  • Acute emphysema-like symptoms: symptoms such as dyspnea, cough with sputum , wheeze etc
  • Acute epiglottitis:
  • Acute episodes of Alzheimers-like symptoms: symptoms of Alzheimer's disease such as dementia can occur in bouts
  • Acute episodic COPD-like symptoms: symptoms such as dyspnea, cough with sputum , wheeze etc
  • Acute episodic adhd-like symptoms: ADHD is a neurodevelopmental behavioural disorder affecting 3-5% of the population characterised by 3 main components: hyperactivity, impulsivity and inattention. Some conditions which cause similar symptoms but episodic in nature include
  • Acute episodic concentration difficulty: concentrating difficulty which occurs only during particular periods
  • Acute episodic emphysema-like symptoms: symptoms like cough with sputum and dyspnea
  • Acute erythroleukemia: A rare condition characterized by the presence of abnormal blood cells (erythroblastic precursors) in the bone marrow and blood. The condition is characterized by anemia and generally leads to the development of acute myelogenous leukemia. The acute form has more severe symptoms than the chronic form.
  • Acute expiratory wheeze in children: An acute expiratory wheeze in children is an abnormal whistling sound heard when a child breathes, often on exhalation.
  • Acute expiratory wheeze in infants: An acute expiratory wheeze in children is a condition in which there is an abnormal whistling sound heard when an infant breathes, often on exhalation.
  • Acute fatty liver of pregnancy: A rare complication of pregnancy that can occur in the second half of the pregnancy. It is characterized by excessive fatty deposits in the liver which can be fatal without prompt diagnosis and treatment which involves delivering the baby as soon as possible.
  • Acute feeling of having difficulty concentrating: maybe due to stress or an underlying neurological lesion
  • Acute feet pain: Acute feet pain is the sudden onset of pain in the feet.
  • Acute fibromyalgia-like chronic pain symptoms: a common disorder, is a syndrome composed of a specific set of signs and symptoms
  • Acute fibromyalgia-like symptoms: a common disorder, is a syndrome composed of a specific set of signs and symptoms
  • Acute fibromyalgia-like symptoms in multiple locations: a common disorder, is a syndrome composed of a specific set of signs and symptoms
  • Acute flank pain: acute flank pain refers to sudden onset pain in one side of the body between the upper abdomen and the back
  • Acute flank pain in pregnancy: Acute flank pain in pregnancy is a feeling of discomfort to the sides of the abdomen. This may occur on one side or both, which may give a clue as to its cause.
  • Acute foot pain: Acute foot pain is a condition in which there is a sudden onset of pain in one foot.
  • Acute forearm pain: forearm pathologies which cause acute pain for a short duration
  • Acute forgetfulness: also known as dementia
  • Acute forgetfulness in pregnancy: Acute forgetfulness in pregnancy is the tendency to have difficulty remembering details over the short term.
  • Acute fulminant multiple sclerosis: Malignant Multiple Sclerosis, is a particularly aggressive form of the disease. Thankfully very rare, this highly aggressive form is defined by its swift and relentless decline to significant disability or even death, often within a few weeks or months after the onset of the initial attack. It is characterized by widespread and progressive cerebral white matter destruction or by severe pathological involvement of clinically strategic regions such as brainstem, resulting in bulbar paralysis.
  • Acute gastritis: Acute gastritis is the sudden onset of irritation or inflammation of the stomach.
  • Acute generalized headache in children: Acute generalized headache in children is a condition in which a child experiences a sudden onset of discomfort throughout the head.
  • Acute gerd-like chest pain: must not be overlooked as it may be a medical emergency
  • Acute gerd-like sternum pain: Gerd presents with symptoms such as chest pain, heartburn and dysphagia
  • Acute gerd-like symptoms: conditions which causes symptoms present in GERD such as heartburn, dysphagia and chest pain
  • Acute hay fever-like breathing symptoms: hay fever is caused by pollens of specific seasonal plants, airborne chemicals and dust particles in people who are allergic to these substances
  • Acute hay fever-like cough: hay fever is caused by pollens of specific seasonal plants, airborne chemicals and dust particles in people who are allergic to these substances
  • Acute hay fever-like runny eyes: hay fever is caused by pollens of specific seasonal plants, airborne chemicals and dust particles in people who are allergic to these substances
  • Acute hay fever-like runny nose: hay fever is caused by pollens of specific seasonal plants, airborne chemicals and dust particles in people who are allergic to these substances
  • Acute hay fever-like sneezing symptoms: is caused by pollens of specific seasonal plants, airborne chemicals and dust particles in people who are allergic to these substances
  • Acute headache: Headache, or cephalgia, is defined as diffuse pain in various parts of the head, with the pain not confined to the area of distribution of a nerve.
  • Acute heartburn after eating: food can be the precipitating factor to cause heartburn
  • Acute heartburn after exercise: exercise maybe be a precipitating factor to some conditions presenting with heartburn
  • Acute heartburn pain resistant to treatment: medication may sometimes not help a condition with heartburn
  • Acute heartburn unrelated to eating: acute heartburn which is constant and not related to eating or any other precipitating factor
  • Acute heartburn with acid reflux: acid reflux related disorders
  • Acute heartburn without reflux: acute heartburn not related to reflux diseases
  • Acute heartburn-like chest pain: must not be overlooked as it may be a medical emergency
  • Acute heartburn-like sternum pain: must not be overlooked as it may be a medical emergency
  • Acute hemorrhagic conjunctivitis:
  • Acute hemorrhagic leukoencephalitis: A rare degenerative brain disease where the patient suffers edema, many small hemorrhages, necrosis of blood vessel walls, demyelination of nerve fibers. Histiocytes, lymphocytes and neutrophils also enter the meninges. Symptoms include severe headache, fever, vomiting and sometimes convulsions and unconsciousness. Also called acute hemorrhagic leukoencephalitis.
  • Acute hyperactivity in adults: maybe to due to various causative agents
  • Acute hyperactivity in the workplace: maybe due to stress or an underlying neurological lesion
  • Acute ibd-like abdominal pain: conditions which causes abdominal pain similar to that in case of inflammatory bowel disease
  • Acute ibs-like abdominal pain: conditions which cause acute abdominal pain similar to that in case of inflammatory bowel disease
  • Acute ichthyosis-like facial skin symptoms: rough and dry facial skin
  • Acute injuries of both knees related to sports: Acute injuries of both knees related to sports is the sudden onset of sports-related trauma to the knees.
  • Acute injuries of the knee related to sports: The knee joint is the largest joint in the body, consisting of 4 bones and an extensive network of ligaments and muscles. Injuries to the knee joint are amongst the most common in sporting activities.
  • Acute intermittent forgetfulness: Acute intermittent forgetfulness is difficulty with remembering that occurs off and on.
  • Acute intermittent forgetfulness in pregnancy: Acute intermittent forgetfulness in pregnancy is the tendency to have difficulty remembering details over the short term.
  • Acute intermittent porphyria: A rare inherited metabolic disorder caused by a disturbed porphyrin metabolism resulting in increased production of porphyrin or its precursors. Symptoms include abdominal pain, photosensitivity and neurological disturbances such as seizures, coma, hallucinations and respiratory paralysis.
  • Acute kidney failure: The sudden and acute loss of kidney function
  • Acute leukaemia of ambiguous lineage: A term used to describe a type of leukemia (a blood cancer) where the leukemic cells cannot be determined as myeloid or lymphoid or where both types of cells are present.
  • Acute liver pain: pain due to pathology in the liver
  • Acute liver pain in pregnancy: Acute liver pain in pregnancy is pain under the ribs on the right side of the upper abdomen. This pain may or may not actually arise from the liver, so other potential causes are also listed.
  • Acute lower respiratory conditions: An acute condition that occurs in the lower respiratory tract
  • Acute lung fibrosis symptoms: symptoms such as dyspnea
  • Acute lymphocytic leukemia: A malignant disease that starts suddenly and progresses quickly. It is characterized by a high number of immature cells in the organs, bone marrow and blood. Symptoms include fever, pallor, anorexia, fatigue, anemia, hemorrhage, bone pain, splenomegaly and frequent infections. Also called acute lymphoblastic leukemia.
  • Acute megacaryoblastic leukemia: A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. More specifically, it involves the rapid proliferation of megakaryoblasts (premature form of megakaryocytes).
  • Acute meningitis: Acute meningitis is an inflammation of the brain that presents in an acute fashion. The inflammation may be the result of infective agents such as bacteria, viruses and fungi as well as non-infective agents such as certain drugs. Acute forms of meningitis can develop in within hours or days whereas chronic meningitis develops over weeks or months.
  • Acute mercury inhalation: Inhalation of mercury vapor can lead to serious symptoms and even death if sufficient quantities are inhaled. Mercury inhalation is more likely in confined or poorly ventilated spaces. Mercury from a broken thermometer can lead to symptoms if it occurs in a confined space.
  • Acute migraine-like symptoms: conditions which causes severe headache
  • Acute mountain sickness: A condition that occurs when an un-acclimatized person climbs to high altitudes.
  • Acute myeloblastic leukemia type 1: A form of blood cancer resulting in the rapid proliferation of immature blood cells (blast cells).
  • Acute myeloblastic leukemia type 2: A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes.
  • Acute myeloblastic leukemia type 3: A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 3 involves the proliferation of promyelocytes.
  • Acute myeloblastic leukemia type 4: A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 4 involves the rapid proliferation of myelocytes and monocytes.
  • Acute myeloblastic leukemia type 5: A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. Type 5 involves the rapid proliferation of monoblasts (immature precursors of monocytes) in particular.
  • Acute myeloblastic leukemia type 6: A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 6 involves the proliferation of the immature precursors of red blood cells called erythroblasts.
  • Acute myeloblastic leukemia type 7: A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. Type 7 involves the rapid proliferation of megakaryoblasts (premature form of megakaryocytes) in particular.
  • Acute myelocytic leukemia: A malignant cancer of blood-forming tissues resulting in a high number of immature leukocytes. Symptoms include soft bleeding gums, anemia, fatigue, fever, dyspnea, moderate splenomegaly, joint and bone pains and frequent infections. Also called acute granulocytic leukemia, acute myelogenous leukemia, acute nonlymphocytic leukemia, myeloid leukemia, splenomedullary leukemia, splenomyelogenous leukemia.
  • Acute myeloid leukaemia and myelodysplastic syndromes related to alkylating agent: The use of alkylating agents to treat cancer can result in leukemia in some patients.
  • Acute myeloid leukaemia and myelodysplastic syndromes related to topoisomerase type II inhibitor: The use of topoisomerase type II inhibitors to treat cancer can result in leukemia in some patients.
  • Acute myeloid leukaemia and myelodysplastic syndromes, therapy related: Certain cancer therapies can result in the development of leukemia in some patients. These therapies includes topoisomerase type II inhibitors and alkylating agents.
  • Acute myeloid leukemia: A form of rapidly progressing blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets.
  • Acute myeloid leukemia, adult: A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets.
  • Acute nausea: The sudden and acute onset of the symptom of nausea
  • Acute nausea and vomiting: Sudden onset unpleasant sensation in the abdomen causing a forcible regurgitation of stomach contents through the mouth
  • Acute nausea and vomiting in pregnancy: Acute nausea and vomiting in pregnancy is the sudden onset of a feeling of sickness in the stomach, associated with vomiting.
  • Acute nausea in pregnancy: Acute nausea in pregnancy is the sudden onset of a feeling of sickness in the stomach, often associated with vomiting.
  • Acute necrotizing ulcerative gingivitis: A reoccurring periodontal disease which results in necrosis and ulceration of the gums. Symptoms may include fever, bone loss, breath odor and enlarge neck and throat lymph nodes. Also called trench mouth, Vincent's angina or Vincent's infection.
  • Acute non lymphoblastic leukemia: A form of rapidly progressing blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets. It is one of the most common forms of leukemia in adults but can occur in children.
  • Acute pain from intercourse: also known as dyspareunia
  • Acute pain from intercourse in pregnancy: Acute pain from intercourse in pregnancy is the sudden onset of pain in the region of the vagina and pelvis, occurring during intercourse whilst pregnant.
  • Acute pain in both cheeks: Acute pain in both cheeks is pain or discomfort that occurs suddenly in both cheeks.
  • Acute pain in both thumbs: Acute pain in both thumbs is discomfort or pain that occurs suddenly in both thumbs.
  • Acute pain in multiple joints: it could be in the form of pain and swelling
  • Acute pain in one cheek: Acute pain in one cheek is discomfort or pain that occurs suddenly in one cheek.
  • Acute pain in the maxillary sinus on both sides: Acute pain in the maxillary sinus on both sides refers to the sudden onset of discomfort or pain that occurs in both maxillary sinuses in the cheekbone areas of the face.
  • Acute pain in the maxillary sinus on one side: Acute pain in the maxillary sinus on pone side refers to the sudden onset of discomfort or pain that occurs in one maxillary sinus in the cheekbone area of one side of the face.
  • Acute pain sitting down: rest pain occurs when blood flow in the extremity falls below resting tissue requirements
  • Acute pain when walking: also known as intermittent claudication
  • Acute pain when walking in pregnancy: Acute pain when walking in pregnancy refers to pain in the region of the hips, lower back and pelvis, occurring in the ambulant woman during pregnancy and often increasing with gestation.
  • Acute pelvic pain in children: Acute pelvic pain in children is a condition in which there is a sudden onset of pain or discomfort in the pelvis of a child.
  • Acute pharyngitis: A condition which is characterized by an acute inflammatory reaction of the pharynx
  • Acute pimples on cheek: acne is a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acute pimples on ears: acne is a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acute pimples on forehead: acne is a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acute pimples on lips: acne is a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acute pimples on nose: acne is a disorder of the pilosebaceous unit. The inflammatory process varies from a papule, pustule to a nodule
  • Acute posterior multifocal placoid pigment: A rare eye disease where the central vision in one or both eyes is affected by inflammation or fluid build up in the retina. The retina lies at the back of the eye. Symptoms such as fever, headache and malaise often precede the eye symptoms. The cause of the condition is unknown but may have autoimmune origins.
  • Acute promyelocytic leukemia: A rare bone marrow cancer characterized by a lack of mature blood cells and excessive amounts of immature blood cells (promyelocytes).
  • Acute prostate pain symptoms: conditions which cause acute pain similar to that of pain due to a prostatic pathology
  • Acute psoriasis-like facial rash: Psoriasis is a noncontagious skin disorder that most commonly appears as inflamed, edematous skin lesions covered with a silvery white scale. The most common type of psoriasis is plaque psoriasis. Psoriasis like plaques on the face may be seen in a few cases such as
  • Acute pulmonary fibrosis-like symptoms: symptoms such as dyspnea

Conditions listing medical symptoms: Head symptoms:

The following list of conditions have 'Head 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.

Select from the following alphabetical view of conditions which include a symptom of Head symptoms or choose View All.

View All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z #

Conditions listing medical complications: Head symptoms:

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

 

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise