Search Ontology:
Human Disease
cone-rod dystrophy 16
- Term ID
- DOID:0111022
- Synonyms
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- CORD16
- retinal dystrophy with early macular involvement
- Definition
- A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22. https://www.ncbi.nlm.nih.gov/pubmed/26865426
- References
- Ontology
- Human Disease ( DOID:0111022 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models