Disease association ontology term - MONDO:0014166 - paroxysmal nocturnal hemoglobinuria 2
Term summary
- ID
- MONDO:0014166
- Name
- paroxysmal nocturnal hemoglobinuria 2
- Ontology or CV name
- Disease association
- Definition
- Any paroxysmal nocturnal hemoglobinuria in which the cause of the disease is a mutation in the PIGT gene.
