Disease Directory

Familial cystic renal disease is an inherited form of cystic kidney disease in which changes in the genome lead to the development of kidney cysts. As...

Familial digital arthropathy-brachydactyly is an inherited condition primarily affecting the joints of the fingers and toes, with a characteristic sho...

Familial dilated cardiomyopathy is a genetic form of heart disease in which the heart muscle becomes thin and weakened, leading to an enlarged chamber...

Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen. This...

Familial flecked retinopathy is an inherited condition that affects the retina, leading to distinctive fleck-like changes that may impact vision. The...

Familial focal alopecia is an inherited condition characterized by patchy hair loss affecting localized areas of the scalp. Although the precise biolo...

Familial generalized lentiginosis is a rare inherited skin disorder characterized by the development of numerous lentigines, which are small, brown to...

Familial gestational hyperthyroidism is an inherited condition affecting thyroid function and overall endocrine regulation. It is associated with path...

Familial glucocorticoid deficiency is a group of primary adrenal insufficiencies in which the adrenal glands fail to produce adequate levels of cortis...

Familial hemiplegic migraine is a migraine disorder characterized by episodes of aura that may include motor weakness. It is a condition with a clear...