Paroxysmal nocturnal hemoglobinuria 2

Definition

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

Also known as 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, PIGT paroxysmal nocturnal hemoglobinuria — per MONDO

Also identified as

• OMIM 615399 per MONDO
• UMLS C3809369 per MONDO