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Disease association ontology term - MONDO:0010438 - paroxysmal nocturnal hemoglobinuria 1

Term summary

ID
MONDO:0010438
Name
paroxysmal nocturnal hemoglobinuria 1
Ontology or CV name
Disease association
Definition
Any paroxysmal nocturnal hemoglobinuria in which the cause of the disease is a mutation in the PIGA gene.

Parents

Annotation

Disease association

MONDO:0010438 - paroxysmal nocturnal hemoglobinuria 1

References:

Genes: