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DOID:0111015 - Newfoundland cone-rod dystrophy
Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the RLBP1 gene on chromosome 15q26.
Synonyms: NFRCD,
Echinobase Genes :
MIM:607476 - newfoundland rod-cone dystrophy; nfrcd |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
cone-rod dystrophy (is_a)