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 )
- is a type of
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