Search Ontology:
Human Disease

cone-rod dystrophy 15

Term ID
DOID:0111021
Synonyms
  • CORD15
Definition
A cone-rod dystrophy that has_material_basis_in homozygous mutation in the CDHR1 gene on chromosome 10q23. https://www.ncbi.nlm.nih.gov/pubmed/20805371
References
Ontology
Human Disease   ( DOID:0111021 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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