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DO Term : achromatopsia 2 [DOID:0110007] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.
  • synonyms:
  • RMCH2,
  • MESH:C536128,
  • rod monochromacy 2,
  • ACHM2,
  • rod monochromatism 2,
  • 216900,
  • GARD:9649,
  • OMIM:216900
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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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