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Disease Index

9,486 diseases

familial infantile gigantism

familial infantile myoclonic epilepsy

familial intestinal malrotation-facial anomalies syndrome

familial intrahepatic cholestasis

instance of intrahepatic cholestasis that is caused by an inherited modification of the individual's genome

familial isolated arrhythmogenic right ventricular dysplasia

familial isolated arrhythmogenic ventricular dysplasia, biventricular form

familial isolated arrhythmogenic ventricular dysplasia, left dominant form

familial isolated arrhythmogenic ventricular dysplasia, right dominant form

familial isolated clinodactyly of fingers

familial isolated deficiency of vitamin E

rare autosomal recessive neurodegenerative disease. Symptoms are similar to those of Friedreich ataxia

familial isolated dilated cardiomyopathy

Familial isolated dilated cardiomyopathy is a rare, genetically heterogeneous cardiac disease characterized by dilatation leading to systolic and diastolic dysfunction of the left and/or right ventricles, causing heart failure or arrhythmia

familial isolated hypoparathyroidism due to impaired PTH secretion

familial isolated pituitary adenoma

familial isolated trichomegaly

familial juvenile gout

kidney disease that is characterized by hyperuricemia with renal uric acid under-excretion, gout and chronic kidney disease

familial keratoacanthoma

familial lambdoid synostosis

familial lipoprotein lipase deficiency

familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides

familial male-limited precocious puberty

familial median cleft of the upper and lower lips

familial Mediterranean fever

familial medullary thyroid carcinoma

thyroid medullary carcinoma that has material basis in autosomal dominant inheritance

familial mesial temporal lobe epilepsy with febrile seizures

familial mitral valve prolapse

instance of mitral valve prolapse (disease) that is caused by an inherited modification of the individual's genome

familial multinodular goiter

instance of multinodular goiter that is caused by an inherited modification of the individual's genome

familial multiple fibrofolliculoma

Familial multiple fibrofolliculoma is a genodermatosis characterised by the presence of multiple hamartomas of the hair follicle. It has been described in one family so far.

familial multiple lipomatosis

rare autosomal disorder characterized by numerous encapsulated lipomas on the trunk and extremities

MeSH: D000071070

familial multiple meningioma

familial nasal acilia

medical condition

familial nephrotic syndrome

Page 113 of 317 (9,486 total)

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