OBO ID: DOID:0111022
Term Name: cone-rod dystrophy 16 Search Ontology:
Synonyms:
  • 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 )
Relationships
is a type of:
OTHER cone-rod dystrophy 16 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
C8orf37 Retinitis pigmentosa 64 614500
Cone-rod dystrophy 16 614500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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