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Congenital Myopathy 19

Disease ID: disease_node_18954

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DbxrefMIM:618578
SubclassofDOID_0050737, DOID_0081337
Data SourceDOID
Doid Labelcongenital myopathy 19
Doid DescriptionA congenital myopathy that is characterized by infantile-onset of progressive muscle weakness and atrophy associated with scoliosis, variably impaired walking, and dysmorphic facial features and that has_material_basis_in homozygous mutation in the PAX7 gene on chromosome 1p36.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_18954
Doid IdDOID_0081351
LabelCongenital Myopathy 19