Disease-gene associations mined from literature

Human genes for Charcot-Marie-Tooth disease

Charcot-Marie-Tooth disease [DOID:10595]

Charcot–Marie–Tooth disease- (CMT), known also as Morbus Charcot-Marie-Tooth, Charcot-Marie-Tooth neuropathy, hereditary motor and sensory neuropathy (HMSN), hereditary sensorimotor neuropathy (HSMN), or peroneal muscular atrophy, is an inherited disorder of nerves (neuropathy) that takes different forms. It is characterized by loss of muscle tissue and touch sensation, predominantly in the feet and legs but also in the hands and arms in the advanced stages of disease. Currently incurable, this disease is one of the most common inherited neurological disorders.

Synonyms:  Charcot-Marie-Tooth disease,  CharcotMarieTooth disease,  Charcot-Marie-Tooth disorder,  Charcot-Marie-Tooth syndrome,  DOID:10595 ...

Linkouts:  OMIM #1 #2 #3 #4 #5