Disease Directory

Waardenburg syndrome type 2B (WS2B) is a rare genetic disorder that is a subtype of Waardenburg syndrome. It is associated with changes in the WS2B ge...

Waardenburg syndrome type 2C is a rare genetic condition that affects pigment in the hair, skin, and eyes, and it is often associated with congenital...

Waardenburg syndrome type 2D is a rare genetic condition that is part of the Waardenburg syndrome family. This group of disorders is known for affecti...

Waardenburg syndrome type 2E is a form of Waardenburg syndrome type 2 that is caused by a mutation in the SOX10 gene. This condition may present with...

Waardenburg syndrome type 3 (WS3) is a very rare subtype of Waardenburg syndrome. It is known for its combination of limb anomalies and congenital hea...

Waardenburg syndrome type 4A is a rare genetic condition that is a subtype of Waardenburg syndrome type 4, also known as Waardenburg-Shah syndrome. Th...

Waardenburg syndrome type 4B is a form of Waardenburg syndrome type 4, also known as Waardenburg-Shah syndrome. It is caused by mutations in the EDN3...

Waardenburg syndrome type 4C is a rare genetic condition that is a subtype of Waardenburg syndrome type 4, also known as Waardenburg-Shah syndrome. Th...

Waardenburg syndrome, IIa 2F is a rare genetic condition that falls under the broader group of Waardenburg syndromes. Although detailed clinical descr...

Waardenburg-Shah syndrome (WSS) is a condition that combines features of Waardenburg syndrome and Hirschsprung disease. People with Waardenburg syndro...

Wagner disease is a rare hereditary eye condition that affects the vitreous, the clear gel in the eye. It is known for causing changes in the vitreous...

Waldenstrom macroglobulinemia is a type of lymphoma characterized by the overproduction of a monoclonal immunoglobulin M protein and manifestations in...

Warburg micro syndrome is a rare, autosomal recessive disorder that mainly affects the eyes, brain, and reproductive system. People with this conditio...

Warburg micro syndrome 1 is a rare genetic condition that is caused by a mutation in the RAB3GAP1 gene. This condition is one of several types of Warb...

Warburg micro syndrome 2 is a rare condition that is a type of Warburg micro syndrome. It is caused by a mutation in the RAB3GAP2 gene. This means tha...

Warburg micro syndrome 3 is a rare genetic condition that is caused by a mutation in the RAB18 gene. It is one form of Warburg micro syndrome. People...

Warburg micro syndrome 4 is a rare genetic condition caused by a mutation in the TBC1D20 gene. It is one form of Warburg micro syndrome, a group of di...

Warsaw breakage syndrome is a rare genetic disorder that mainly affects growth, resulting in severe growth retardation and a smaller than expected hea...

Waterhouse-Friderichsen syndrome is a serious condition in which there is massive bleeding into the adrenal glands. It occurs mainly as a result of a...

Watson syndrome is considered a variant of neurofibromatosis type 1. It is most noted for its unique combination of features including heart valve pro...