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Summary Literature (0)
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 : nr2e3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012625 - retinitis pigmentosa 37

MIM:
MIM:611131 - RETINITIS PIGMENTOSA 37; RP37

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), retinitis pigmentosa (is_a)