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Charcot-Marie-Tooth disease type 2Y

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any Charcot-Marie-Tooth disease type 2 in which the cause of the disease is a mutation in the VCP gene.
Uniprot Description An autosomal dominant, axonal form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathies (designated CMT1 when they are dominantly inherited) and primary peripheral axonal neuropathies (CMT2). Neuropathies of the CMT2 group are characterized by signs of axonal degeneration in the absence of obvious myelin alterations, normal or slightly reduced nerve conduction velocities, and progressive distal muscle weakness and atrophy.
Disease Ontology Description A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the VCP gene on chromosome 9p13.
Mondo Term and Equivalent IDs
MONDO:0014735:  Charcot-Marie-Tooth disease type 2Y
Orphanet:435387: 
UMLS:C4225244: