OBO ID: DOID:0110007
Term Name: achromatopsia 2 Search Ontology:
Synonyms:
  • ACHM2
  • RMCH2
  • rod monochromacy 2
  • rod monochromatism 2
Definition: An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11. (2)
References:
Ontology: Human Disease   ( DOID:0110007 )
Relationships
is a type of:
OTHER achromatopsia 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CNGA3 Achromatopsia 2 216900
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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