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Myopathies, Structural, Congenital

Disease ID: disease_node_10806

Connections displayed (default: 10).
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DbxrefGARD:12719, ICD10CM:G71.228, MESH:D020914, ORDO:169189, SNOMEDCT_US_2023_03_01:716696006, UMLS_CUI:C1834558
SubclassofDOID_0050736, DOID_14717
Data SourceDOID, MESH
SynonymsAD-CNM
Mesh IdD020914
Mesh LabelMyopathies, Structural, Congenital
Mesh SubclassofD009135
Doid Labelautosomal domit centronuclear myopathy
Doid DescriptionA centronuclear myopathy that has_material_basis_in autosomal domit inheritance.
Has Material Basis InGENO_0000147
Disease Node Iddisease_node_10806
Doid IdDOID_0111217
LabelMyopathies, Structural, Congenital