Paroxysmal nocturnal hemoglobinuria 2

MONDO:0014166

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

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