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Disease association ontology term - MONDO:0012943 - retinitis pigmentosa 46

Term summary

ID
MONDO:0012943
Name
retinitis pigmentosa 46
Ontology or CV name
Disease association
Definition
Any retinitis pigmentosa in which the cause of the disease is a mutation in the IDH3B gene.

Parents

Annotation

Disease association

MONDO:0012943 - retinitis pigmentosa 46

References:

Genes: