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Disease association ontology term - MONDO:0012363 - retinitis pigmentosa 32

Term summary

ID
MONDO:0012363
Name
retinitis pigmentosa 32
Ontology or CV name
Disease association
Definition
A retinitis pigmentosa that has material basis in variation in the chromosome region 1p21.3-p13.3.

Parents

Annotation

Disease association

MONDO:0012363 - retinitis pigmentosa 32

References:

Genes: