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Summary Literature (1)
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

Xenbase Genes : abca4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011137 - axial skeletal system

MIM:
MIM:601718 - RETINITIS PIGMENTOSA 19; RP19

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

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