Search Ontology:
Human Disease
retinitis pigmentosa 38
- Term ID
- DOID:0110367
- Synonyms
-
- RP38
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13. https://www.ncbi.nlm.nih.gov/pubmed/11062461
- References
-
- ICD10CM:H35.5
- MIM:613862
- Ontology
- Human Disease ( DOID:0110367 )
- is a type of
-
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Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| MERTK | Retinitis pigmentosa 38 | retinitis pigmentosa 38 | 613862 |
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Zebrafish Models