Search Ontology:
Human Disease
retinitis pigmentosa 83
- Term ID
- DOID:0112140
- Synonyms
-
- RP83
- Definition
- A retinitis pigmentosa characterized by onset of night blindness in the first decade of life, decreased central vision in the second decade of life, and retinal degeneration that has_material_basis_in heterozygous mutation in ARL3 on chromosome 10q24.32. https://pubmed.ncbi.nlm.nih.gov/30932721/
- References
- Ontology
- Human Disease ( DOID:0112140 )
- is a type of
-
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Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| ARL3 | Retinitis pigmentosa 83 | retinitis pigmentosa 83 | 618173 |
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Zebrafish Models
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