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DOID:0111523 - autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3
Disease Ontology Definition:A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in TK2 on chromosome 16q21.
Synonyms: PEOB3, autosomal recessive progressive external ophthalmoplegia 3,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee