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Summary Literature (0)
DOID:0110357 - retinitis pigmentosa 35

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the SEMA4A gene on chromosome 1q22.

Synonyms: RP35

Xenbase Genes : sema4a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012463 - retinitis pigmentosa 35


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

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