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DOID:0110399 - retinitis pigmentosa 37
Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23.
Synonyms: RP37
Xenbase Genes

MONDO:0012625 - retinitis pigmentosa 37 |
OMIM:611131 - RETINITIS PIGMENTOSA 37; RP37 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
retinitis pigmentosa (is_a)