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Disease association ontology term - MONDO:0800393 - IDH3B-related retinopathy

Term summary

ID
MONDO:0800393
Name
IDH3B-related retinopathy
Ontology or CV name
Disease association
Definition
An inherited retinopathy caused by bi-allelic variants in the IDH3B gene.

Parents

Annotation

Disease association

MONDO:0012943 - retinitis pigmentosa 46

References:

Genes: