Search Ontology:
Human Disease
cone-rod dystrophy 24
- Term ID
- DOID:0081449
- Synonyms
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- Definition
- A cone-rod dystrophy that is characterized by night blindness, defective color vision, and reduced visual acuity and that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11. https://pubmed.ncbi.nlm.nih.gov/35947183/
- References
- Ontology
- Human Disease ( DOID:0081449 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models