Search Ontology:
Human Disease
retinitis pigmentosa 41
- Term ID
- DOID:0110376
- Synonyms
-
- RP41
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the PROM1 gene on chromosome 4p15. https://www.ncbi.nlm.nih.gov/pubmed/10587575
- References
-
- ICD10CM:H35.5
- MESH:C567422
- MIM:612095
- Ontology
- Human Disease ( DOID:0110376 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models