OBO ID: DOID:0111005
Term Name: cone-rod dystrophy 2 Search Ontology:
Synonyms:
  • cone-rod retinal dystrophy 2
  • CORD2
  • CRD2
  • RCRD2
  • retinal cone-rod dystrophy 2
Definition: A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/9390563
References:
Ontology: Human Disease   ( DOID:0111005 )
Relationships
is a type of:
disjoint_from:
OTHER cone-rod dystrophy 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CRX Cone-rod retinal dystrophy-2 120970
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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