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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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory