Search Ontology:
Human Disease

cone-rod dystrophy 6

Term ID
DOID:0111011
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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