Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Inherited thrombocytopenia
Thrombocytopenia 2
An autosomal dominant disorder caused by mutation(s) in the ANKRD26 gene, encoding ANKRD26 protein. Additionally, in one family, a mutation(s) has been identified in the MASTL gene, encoding serine/threonine-protein kinase greatwall. The condition is characterized by mild to moderate bruisability.
This condition has no sub-types.