OBO ID: DOID:0111435
Term Name: optic atrophy 6 Search Ontology:
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 optic atrophy 6 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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