OBO ID: DOID:0111017
Term Name: cone-rod dystrophy 10 Search Ontology:
Synonyms:
  • CORD10
Definition: A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22. https://www.ncbi.nlm.nih.gov/pubmed/16199541
References:
Ontology: Human Disease   ( DOID:0111017 )
OTHER cone-rod dystrophy 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SEMA4A Cone-rod dystrophy 10 610283
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None