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Disease association ontology term - MONDO:0003608 - optic atrophy

Term summary

ID
MONDO:0003608
Name
optic atrophy
Ontology or CV name
Disease association
Definition
A disorder characterized by loss of optic nerve fibers. It may be inherited or acquired. Acquired causes include ischemia, optic nerve neuropathy, glaucoma, trauma, radiation, brain tumors, and multiple sclerosis. It leads to vision disturbances.

Parents

Annotation

Disease association

MONDO:0003608 - optic atrophy

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MONDO:0014720 - autosomal dominant optic atrophy plus syndrome

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MONDO:0008134 - autosomal dominant optic atrophy, classic form

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MONDO:0020737 - optic atrophy 10 with or without ataxia, intellectual disability, and seizures

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MONDO:0015011 - optic atrophy 11

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MONDO:0033549 - optic atrophy 12

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MONDO:0008135 - optic atrophy 13 with retinal and foveal abnormalities

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MONDO:0957935 - optic atrophy 15

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MONDO:0957978 - optic atrophy 16

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MONDO:0008133 - optic atrophy 3

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MONDO:0012543 - optic atrophy 5

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MONDO:0014571 - optic atrophy 9

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

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