Search Ontology:
Human Disease

optic atrophy 2

Term ID
DOID:0111443
Synonyms
  • OPA2
  • X-linked optic atrophy 2
Definition
An optic atrophy that has_material_basis_in variation in a region on chromosome Xp11.4-p11.21. https://www.ncbi.nlm.nih.gov/pubmed/9382106
References
Ontology
Human Disease   ( DOID:0111443 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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