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Charcot-Marie-Tooth Disease Type 4

Disease ID: disease_node_18827

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DbxrefGARD:12440, ORDO:64749
SubclassofDOID_10595
Data SourceDOID
Synonymshereditary motor and sensory neuropathy
Doid LabelCharcot-Marie-Tooth disease type 4
Doid DescriptionA Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance. Xref MGI. OMIM mapping confirmed by DO. [SN].
Disease Node Iddisease_node_18827
Doid IdDOID_0050541
LabelCharcot-Marie-Tooth Disease Type 4
Doid Alternate IdsDOID_0050582