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DO Term : achromatopsia 7 [DOID:0110009] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23.

synonyms:
616517,
ACHM7,
OMIM:616517

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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