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Disease association ontology term - MONDO:0020250 - autosomal dominant optic atrophy

Term summary

ID
MONDO:0020250
Name
autosomal dominant optic atrophy
Ontology or CV name
Disease association
Definition
An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss.

Parents

Annotation

Disease association

MONDO:0014720 - autosomal dominant optic atrophy plus syndrome

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Genes:

MONDO:0008134 - autosomal dominant optic atrophy, classic form

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MONDO:0008133 - optic atrophy 3

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MONDO:0012543 - optic atrophy 5

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MONDO:0007429 - optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy

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