Search Ontology:
Human Disease
retinitis pigmentosa 32
- Term ID
- DOID:0110355
- Synonyms
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- RP32
- Definition
- A retinitis pigmentosa that has_material_basis_in variation in the chromosome region 1p21.3-p13.3. https://www.ncbi.nlm.nih.gov/pubmed/16189710
- References
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- ICD10CM:H35.5
- MESH:C563689
- MIM:609913
- Ontology
- Human Disease ( DOID:0110355 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models