Search Ontology:
Human Disease
retinitis pigmentosa 33
- Term ID
- DOID:0110366
- Synonyms
-
- RP33
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11. https://www.ncbi.nlm.nih.gov/pubmed/19878916
- References
-
- ICD10CM:H35.5
- MESH:C563676
- MIM:610359
- Ontology
- Human Disease ( DOID:0110366 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models