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DOID:0110377 - retinitis pigmentosa 49
Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the CNGA1 gene on chromosome 4p12.
Synonyms: RP49,
Echinobase Genes :
MIM:613756 - retinitis pigmentosa 49; rp49 |
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)