Search Ontology:
Human Disease

achromatopsia 3

Term ID
DOID:0110008
Synonyms
  • ACHM1
  • ACHM3
  • Pingelapese blindness
  • RMCH1
  • rod monochromacy 1
  • rod monochromatism 1
Definition
An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2. (2)
References
Ontology
Human Disease   ( DOID:0110008 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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