OBO ID: DOID:0111011
Term Name: cone-rod dystrophy 6 Search Ontology:
Synonyms:
  • CORD6
  • RCD2
  • retinal cone dystrophy 2
Definition: A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the GUCY2D gene on chromosome 17p13.1. https://www.ncbi.nlm.nih.gov/pubmed/9618177
References:
Ontology: Human Disease   ( DOID:0111011 )
Relationships
is a type of:
OTHER cone-rod dystrophy 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GUCY2D Cone-rod dystrophy 6 601777
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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