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Disease Ontology Browser
retinitis pigmentosa (DOID:10584)
Alliance: disease page
Synonyms: pericentral pigmentary retinopathy
Alt IDs: DOID:14742, ICD10CM:H35.52, MESH:C538365, MESH:D012174, NCI:C85045, OMIM:PS268000, ORDO:791, UMLS_CUI:C0035334, UMLS_CUI:C0220701
Definition: A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss.

Disease References using Mouse Models (95)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.13
The Jackson Laboratory