Search Ontology:
Human Disease

autosomal recessive progressive external ophthalmoplegia 1

Term ID
DOID:0111522
Synonyms
  • PEOB1
Definition
A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the POLG gene on chromosome 15q26.1. https://www.ncbi.nlm.nih.gov/pubmed/11431686
References
Ontology
Human Disease   ( DOID:0111522 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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