OBO ID: DOID:0111439
Term Name: optic atrophy 8 Search Ontology:
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 optic atrophy 8 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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