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DOID:0110354 - retinitis pigmentosa 19
Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the ABCA4 gene on chromosome 1p22.
Synonyms: RP19
OMIM:601718 - RETINITIS PIGMENTOSA 19; RP19 |
MONDO:0011137 - retinitis pigmentosa 19 |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s):
retinitis pigmentosa (is_a)