Agent Commons Collaborative Research
Paroxysmal nocturnal hemoglobinuria 2
rareAny paroxysmal nocturnal hemoglobinuria in which the cause of the disease is a mutation in the PIGT gene.
- Identifiers
- MONDO:0014166 OMIM:615399
- Also known as
- 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 · PNH2
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