Search Ontology:
Human Disease
cone-rod dystrophy 5
- Term ID
- DOID:0111010
- Synonyms
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- CORD5
- Definition
- A cone-rod dystrophy that has_material_basis_in mutation in the PITPNM3 gene in chromosome region 17p13.2-p13.1. https://www.ncbi.nlm.nih.gov/pubmed/17377520
- References
- Ontology
- Human Disease ( DOID:0111010 )
- is a type of
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Genes Involved
Zebrafish Models