Search Ontology:
Human Disease

achromatopsia 2

Term ID
DOID:0110007
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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