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DOID:0110406 - retinitis pigmentosa 30
Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25.
Synonyms: RP30,
Echinobase Genes :
MIM:607921 - retinitis pigmentosa 30; rp30 macular degeneration, 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)