OBO ID: DOID:0111021
Term Name: cone-rod dystrophy 15 Search Ontology:
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 cone-rod dystrophy 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDHR1 Retinitis pigmentosa 65 613660
Cone-rod dystrophy 15 613660
Macular dystrophy, retinal 613660
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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