Bernard-Soulier syndrome, type A2, autosomal dominant

MONDO:0007930

A Bernard-Soulier syndrome characterized by autosomal dominant inheritance of mild to moderate bleeding tendency, thrombocytopenia, and an increased mean platelet size that has material basis in heterozygous mutations in the GP1BA gene on chromosome 17p.

Also known as: BSSA2, Bernard-Soulier syndrome, type A2 (dominant), Bernard-Soulier syndrome, type A2, autosomal dominant, Bernard-Soulier syndrome type A2

10 clinical trials for this condition and its sub-types, 0 tagged with Bernard-Soulier syndrome, type A2, autosomal dominant itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Bernard-Soulier syndrome (0)

Including sub-types (10) Tagged with Bernard-Soulier syndrome, type A2, autosomal dominant (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.