Search Ontology:
Human Disease

achromatopsia 4

Term ID
DOID:0110010
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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