Search Ontology:
Human Disease
retinitis pigmentosa 20
- Term ID
- DOID:0110353
- Synonyms
-
- RP20
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the RPE65 gene on chromosome 1p31. https://www.ncbi.nlm.nih.gov/pubmed/9326941
- References
-
- ICD10CM:H35.5
- MESH:C566718
- MIM:613794
- Ontology
- Human Disease ( DOID:0110353 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models