bn:00017784n
Noun Concept
Categories: Syndromes affecting the nervous system, Sensory systems, Cytoskeletal defects, Articles with short description, Neurological disorders
EN
hereditary motor and sensory neuropathy  Charcot-Marie-Tooth disease  Charcot–Marie–Tooth disease
EN
A form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant WordNet 3.0
Definitions
Relations
Sources
EN
A form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant WordNet 3.0 & WordNet 2020
Hereditary motor and sensory neuropathies is a name sometimes given to a group of different neuropathies which are all characterized by their impact upon both afferent and efferent neural communication. Wikipedia
Charcot–Marie–Tooth disease is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle tissue and touch sensation across various parts of the body. Wikipedia
Neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm Wikidata
Congenital disorder of nervous system Wikidata
Wikipedia Redirections
EN
AR-CMT2, Carcot marie tooth, Charcot-Marie-Tooth, Charcot-Marie-Tooth Disease, Charcot-marie-tooth disease, Charcot-Marie-tooth disease, Charcot-Marie-Tooth disease, Charcot-Marie-Tooth disease, neuronal, type A, Charcot-Marie-Tooth disease, neuronal, type B, Charcot-Marie-Tooth disease, neuronal, type D, Charcot-Marie-Tooth disease, type 1, Charcot-Marie-Tooth disease, type 2, Charcot-Marie-Tooth disease, type 4, Charcot-Marie-Tooth disease, X-linked recessive, 4, Charcot-Marie-Tooth disease, X-linked recessive type 5, Charcot-Marie-Tooth disease, X-linked type 1, Charcot-Marie-Tooth disease, X-linked type 2, recessive, Charcot-Marie-Tooth disease, X-linked type 2 recessive, Charcot-Marie-Tooth disease, X-linked type 3, recessive, Charcot-Marie-Tooth disease, X-linked type 3 recessive, Charcot-Marie-Tooth disease 2B1, Charcot-Marie-Tooth disease and deafness deafness dominant type, Charcot-Marie-Tooth disease deafness dominant type, Charcot-Marie-Tooth disease deafness recessive type, Charcot-Marie-Tooth disease type 1, Charcot-Marie-Tooth disease type 1 aplasia cutis congenita, Charcot-Marie-Tooth disease type 1A, Charcot-Marie-Tooth disease type 1B, Charcot-Marie-Tooth disease type 1C, Charcot-Marie-Tooth disease type 1D, Charcot-Marie-Tooth disease type 1E, Charcot-Marie-Tooth disease type 1F, Charcot-Marie-Tooth disease type 2, Charcot-Marie-Tooth disease type 2A, Charcot-Marie-Tooth disease type 2A1, Charcot-Marie-Tooth disease type 2A2, Charcot-Marie-Tooth disease type 2B, Charcot-Marie-Tooth disease type 2B1, Charcot-Marie-Tooth disease type 2B2, Charcot-Marie-Tooth disease type 2C, Charcot-Marie-Tooth disease type 2D, Charcot-Marie-Tooth disease type 2E, Charcot-Marie-Tooth disease type 2I, Charcot-Marie-Tooth disease type 2J, Charcot-Marie-Tooth disease type 4A, Charcot-Marie-Tooth disease type 4B, Charcot-Marie-Tooth disease type 4C, Charcot-Marie-Tooth disease type 4D, Charcot-Marie-Tooth disease type 4F, Charcot-Marie-Tooth disease type 4H, Charcot-Marie-Tooth disease type 4J, Charcot-Marie-Tooth disease with deafness and mental retardation, Charcot-Marie-Tooth disease with ptosis and parkinsonism, Charcot-Marie-Tooth neuropathy, Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, Charcot-Marie-Tooth peroneal muscular atrophy X-linked, Charcot-Marie-Tooth syndrome, Charcot-Marie-Tooth syndrome type 1A, Charcot-Marie-Tooth type 1 aplasia cutis congenita, Charcot-Marie Tooth Disease, Charcot marie tooth, Charcot Marie Tooth disease, Charcot Marie Tooth disease deafness dominant type, Charcot Marie tooth disease deafness dominant type, Charcot Marie tooth disease deafness mental retardation, Charcot Marie Tooth disease deafness recessive type, Charcot Marie tooth disease with deafness and mental retardation, Charcot Marie Tooth type 1 aplasia cutis congenita, Charcot–Marie–Tooth disease, type 1, Charcot–Marie–Tooth disease, type 2, Charcot–Marie–Tooth disease, type 4, Charcot–Marie–Tooth disease 2B1, Charcot–Marie–Tooth syndrome type 1A, Cmt1a, CMT2A, CMT4, CMT5, CMT6, CMTD, CMTDI, CMTRI, Cowchock Syndrome, Cowchock syndrome, Hereditary motor and sensory neuropathies, Hereditary Motor and Sensory Neuropathy, Hereditary motor and sensory neuropathy type 1, Hereditary Motor Sensory Neuropathy, Hereditary motor sensory neuropathy, Hereditary sensorimotor neuropathy, Hereditary sensorimotor neuropathy type 1, Hereditary sensorimotor neuropathy type 2, Hereditary sensory-motor neuropathy type 2, Hereditary Sensory & Motor Neuropathy, Hereditary sensory and motor neuropathy, Hereditary Sensory and Motor Neuropathy, Hereditary sensory motor neuropathy, Hereditary Sensory Motor Neuropathy, HMSN, HSMN type 1, HSMN type 2, Motor sensory neuropathy type 1 aplasia cutis congenita, Neuropathy, axonal motor-sensory with deafness and mental retardation, Peroneal Muscle Atropy, Peroneal muscular atrophy, Peroneal Muscular Atrophy, Peroneal muscular atrophy type 1, Peroneal muscular atrophy type 2, Rosenberg-Chutorian syndrome, Rosenberg Chutorian syndrome, Rosenberg–Chutorian syndrome