Search Ontology:
Human Disease

achromatopsia 7

Term ID
DOID:0110009
Synonyms
  • ACHM7
Definition
An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23. (2)
References
Ontology
Human Disease   ( DOID:0110009 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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