Search Ontology:
Human Disease

optic atrophy 6

Term ID
DOID:0111435
Synonyms
  • OPA6
Definition
An optic atrophy characterized by early onset of slowly progressive isolated optic atrophy that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 8q21-q22. https://www.ncbi.nlm.nih.gov/pubmed/14508503
References
Ontology
Human Disease   ( DOID:0111435 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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