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DOID:0110388 - retinitis pigmentosa 10
Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the IMPDH1 gene on chromosome 7q32.
Synonyms: RP10,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:180105 - retinitis pigmentosa 10; rp10 |
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)