OBO ID: DOID:0110009
Term Name: achromatopsia 7 Search Ontology:
Synonyms:
  • ACHM7
Definition: An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23. (2)
References:
Ontology: Human Disease   (DOID:0110009)
OTHER achromatopsia 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ATF6 Achromatopsia 7 616517
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None