Disease Directory

Basal cell nevus syndrome 1 is a genetic condition that primarily affects the skin and craniofacial structures, and it is also associated with variabl...

Basal cell nevus syndrome 2 is a complex condition that primarily affects the skin and head, with a high likelihood of developing multiple basal cell...

basal encephalocele is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Basal ganglia calcification, idiopathic, 1 is a neurological condition characterized by abnormal calcium deposits in the basal ganglia, a key region i...

Basal ganglia calcification, idiopathic, 10, autosomal recessive is a neurological condition characterized by abnormal calcium deposits in various reg...

Basal ganglia calcification, idiopathic, 4 is a neurological condition characterized by abnormal calcium deposits in the basal ganglia. The condition...

Basal ganglia calcification, idiopathic, 5 is a neurological condition primarily characterized by the abnormal deposition of calcium in the basal gang...

Basal ganglia calcification, idiopathic, 6 (IBGC6) is a neurological condition in which deposits of calcium build up in deep brain structures called t...

Basal ganglia calcification, idiopathic, 7, autosomal recessive is a neurological condition characterized by abnormal calcification in deep brain stru...

Basal ganglia calcification, idiopathic, 8, autosomal recessive is a neurological condition primarily characterized by abnormal calcifications in the...

Basal ganglia calcification, idiopathic, 9, autosomal recessive is a neurologically focused condition characterized by abnormal deposits in brain regi...

Basal ganglia calcification, idiopathic, childhood-onset is an extremely rare condition. Because few cases have been documented, detailed clinical inf...

Basal laminar drusen is characterized by yellow-white deposits that accumulate beneath the retinal pigment epithelium on Bruch membrane. This conditio...

Basaloid carcinoma of the penis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Basidiobolomycosis is an extremely rare condition caused by infection with Basidiobolus. Because few cases have been documented, detailed clinical inf...

Bathing suit ichthyosis (BSI) is a distinct variant of congenital ichthyosis marked by the presence of large, dark scales primarily localized to areas...

Behavioral variant of frontotemporal dementia (bv-FTD) is characterized by progressive behavioral impairment and a decline in executive function, prim...

bejel is an extremely rare condition. It is a chronic skin and tissue disease caused by infection with the endemicum subspecies of the spirochete Trep...

benign PEComa is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Benign Samaritan congenital myopathy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.