PomBase home

Disease association ontology term - MONDO:0043878 - hereditary optic atrophy

Term summary

ID
MONDO:0043878
Name
hereditary optic atrophy
Ontology or CV name
Disease association
Definition
A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.

Parents

Annotation

Disease association

MONDO:0014720 - autosomal dominant optic atrophy plus syndrome

References:

Genes:

MONDO:0008134 - autosomal dominant optic atrophy, classic form

References:

Genes:

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

References:

Genes:

MONDO:0015011 - optic atrophy 11

References:

Genes:

MONDO:0033549 - optic atrophy 12

References:

Genes:

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

References:

Genes:

MONDO:0957935 - optic atrophy 15

References:

Genes:

MONDO:0957978 - optic atrophy 16

References:

Genes:

MONDO:0008133 - optic atrophy 3

References:

Genes:

MONDO:0012543 - optic atrophy 5

References:

Genes:

MONDO:0014571 - optic atrophy 9

References:

Genes:

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

References:

Genes: