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Autosomal Domit Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 4

Disease ID: disease_node_18042

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DbxrefMIM:610131
SubclassofDOID_0050736, DOID_12558
Data SourceDOID
SynonymsPEOA4, autosomal dominant progressive external ophthalmoplegia 4
Doid Labelautosomal domit progressive external ophthalmoplegia with mitochondrial DNA deletions 4
Doid DescriptionA chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the POLG2 gene on chromosome 17q23.3.
Has Material Basis InGENO_0000147
Disease Node Iddisease_node_18042
Doid IdDOID_0111525
LabelAutosomal Domit Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 4