Search Ontology:
Human Disease
retinitis pigmentosa 59
- Term ID
- DOID:0110352
- Synonyms
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- RP59
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11. https://www.ncbi.nlm.nih.gov/pubmed/21295283
- References
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- ICD10CM:H35.5
- MIM:613861
- Ontology
- Human Disease ( DOID:0110352 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models