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Retinitis pigmentosa 10; RP10

Disease ID:821
Name:Retinitis pigmentosa 10; RP10
Associated with:1 target
Retinitis pigmentosa
Database Links
Disease Ontology: DOID:10584
OMIM: 180105
Orphanet: ORPHA791


inosine monophosphate dehydrogenase 1
References:  1
Mutations:  inosine monophosphate dehydrogenase 1 is associated with 1 mutation. Click here for details


No ligand related data available for Retinitis pigmentosa 10; RP10


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1. Bowne SJ, Sullivan LS, Mortimer SE, Hedstrom L, Zhu J, Spellicy CJ, Gire AI, Hughbanks-Wheaton D, Birch DG, Lewis RA et al.. (2006) Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis. Invest. Ophthalmol. Vis. Sci., 47 (1): 34-42. [PMID:16384941]