OBO ID: DOID:0111013
Term Name: cone-rod dystrophy 3 Search Ontology:
Synonyms:
  • CORD3
Definition: A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ABCA4 gene on chromosome 1p22. https://www.ncbi.nlm.nih.gov/pubmed/9466990
References:
Ontology: Human Disease   ( DOID:0111013 )
OTHER cone-rod dystrophy 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ABCA4 Cone-rod dystrophy 3 604116
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None