retinitis pigmentosa 32 Disease Ontology Browser

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Disease Ontology Browser

retinitis pigmentosa 32 (DOID:0110355)
Alliance: disease page
Synonyms: RP32
Alt IDs: OMIM:609913, ICD10CM:H35.5, MESH:C563689
Definition: A retinitis pigmentosa that has_material_basis_in variation in the chromosome region 1p21.3-p13.3.

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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