Search Ontology:
Human Disease

optic atrophy 8

Term ID
DOID:0111439
Synonyms
  • OPA8
Definition
An optic atrophy characterized by progressive visual loss during the first or second decade of life that has_material_basis_in heterozygous mutation in a region on chromosome 16q21-q22. https://www.ncbi.nlm.nih.gov/pubmed/21349918
References
Ontology
Human Disease   ( DOID:0111439 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models