PomBase home

Disease association ontology term - MONDO:0013468 - retinitis pigmentosa 59

Term summary

ID
MONDO:0013468
Name
retinitis pigmentosa 59
Ontology or CV name
Disease association
Definition
Any retinitis pigmentosa in which the cause of the disease is a mutation in the DHDDS gene.

Parents

Annotation

Disease association

MONDO:0013468 - retinitis pigmentosa 59

References:

Genes: