OBO ID: DOID:0110010
Term Name: achromatopsia 4 Search Ontology:
Synonyms:
  • ACHM4
Definition: An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the GNAT2 gene on chromosome 1p13. https://www.ncbi.nlm.nih.gov/pubmed/12205108
References:
Ontology: Human Disease   ( DOID:0110010 )
Relationships
is a type of:
OTHER achromatopsia 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GNAT2 Achromatopsia 4 613856
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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