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Metadata
ID	DOID:0110009
Name	achromatopsia 7
Definition	An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23. https://www.ncbi.nlm.nih.gov/pubmed/26063662, https://www.ncbi.nlm.nih.gov/pubmed/26029869
Xrefs	MIM:616517
Synonyms	ACHM7 [EXACT]
Parent Relationships	is_a achromatopsia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance