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Charcot-Marie-Tooth disease type 2D

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Mondo Description Autosomal dominant Charcot-Marie-Tooth disease type 2D (CMT2D) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by distal weakness primarily and predominantly occurring in the upper limbs and tendon reflexes absent or reduced in the arms and decreased in the legs. Progression is slow.
Uniprot Description A 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.
Mondo Term and Equivalent IDs
MONDO:0011091:  Charcot-Marie-Tooth disease type 2D
GARD:0001251: 
MESH:C537993: 
NCIT:C122659: 
Orphanet:99938: 
SCTID:717011006: 
UMLS:C1832274: 
UMLS:C4274109: