OBO ID: DOID:0111433
Term Name: optic atrophy 3 Search Ontology:
Synonyms:
  • ADOAC
  • autosomal dominant optic atrophy 3
  • autosomal dominant optic atrophy and cataract
  • autosomal dominant optic atrophy type 3
  • OPA3
  • optic atrophy 3 with cataract
Definition: An optic atrophy characterized by optic atrophy and cataract that has_material_basis_in heterozygous mutation in the OPA3 gene on chromosome 19q13.32. https://www.ncbi.nlm.nih.gov/pubmed/15342707
References:
Ontology: Human Disease   ( DOID:0111433 )
Relationships
is a type of:
OTHER optic atrophy 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
OPA3 Optic atrophy 3 with cataract 165300
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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