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DO Term : autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4 [DOID:0111516] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A chronic progressive external ophthalmoplegia characterized by adult onset of eye muscle weakness and proximal limb muscle weakness that has_material_basis_in homozygous or compound heterozygous mutation in the DGUOK gene on chromosome 2p13.1.
  • synonyms:
  • autosomal recessive progressive external ophthalmoplegia 4,
  • ORDO:329314,
  • 617070,
  • adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency,
  • PEOB4,
  • adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency,
  • OMIM:617070
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