Paroxysmal nocturnal hemoglobinuria 2

Any paroxysmal nocturnal hemoglobinuria in which the cause of the disease is a mutation in the PIGT gene.

Also known as: PIGT paroxysmal nocturnal hemoglobinuria, paroxysmal nocturnal hemoglobinuria 2, paroxysmal nocturnal hemoglobinuria 2, autosomal dominant, somatic mutation, paroxysmal nocturnal hemoglobinuria caused by mutation in PIGT, paroxysmal nocturnal hemoglobinuria type 2, PNH2

8 clinical trials for this condition and its sub-types.