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Human Disease

optic atrophy 12

Term ID
DOID:0080840
Synonyms
Definition
An optic atrophy that is characterized by slowly progressive visual impairment with onset usually in the first decade and that has_material_basis_in heterozygous mutation in the AFG3L2 gene on chromosome 18p11. https://pubmed.ncbi.nlm.nih.gov/32219868/
References
Ontology
Human Disease   ( DOID:0080840 )
Relationships
is a type of
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Genes Involved
Zebrafish Models