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DOID:0110371 - retinitis pigmentosa 56
Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the IMPG2 gene on chromosome 3q12.3.
Synonyms: RP56,
Echinobase Genes :
MIM:613581 - retinitis pigmentosa 56; rp56 maculopathy, impg2-related, included |
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)