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Metadata
ID DOID:0110007
Name achromatopsia 2
Definition An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.
https://www.ncbi.nlm.nih.gov/pubmed/11536077, https://www.ncbi.nlm.nih.gov/pubmed/9662398
Xrefs

GARD:9649

OMIM:216900

Synonyms

ACHM2 [EXACT]

RMCH2 [EXACT]

rod monochromacy 2 [EXACT]

rod monochromatism 2 [EXACT]

Parent Relationships

is_a achromatopsia

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