Search Ontology:
Human Disease
retinitis pigmentosa 89
- Term ID
- DOID:0112146
- Synonyms
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- RP89
- Definition
- A retinitis pigmentosa characterized by onset of retinitis pigmentosa in the first decade of life and additional features of ciliopathy that has_material_basis_in heterozygous mutation in the KIF3B gene on chromosome 20q11.21. https://pubmed.ncbi.nlm.nih.gov/32386558/
- References
- Ontology
- Human Disease ( DOID:0112146 )
- is a type of
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Genes Involved
Zebrafish Models