Charcot-Marie-Tooth disease https://www.malacards.org/card/charcot_marie_tooth_disease https://www.malacards.org/card/charcot_marie_tooth_disease_hereditary_motor_and_sensory_neuropathy Charcot-Marie-Tooth disease NORD:919 NANDO:2200855 OMIMPS:118220 GARD:0006034 Charcot Marie Tooth disease MedDRA:10034699 An inherited degenerative disorder involving the peripheral nerves. It is caused by mutations in the genes that are responsible for the production of proteins necessary for the function and structure of the peripheral nerves. It is characterized by muscle atrophy and weakness in the feet, legs, hands, and arms and loss of sensation in the limbs. peroneal muscular atrophy DOID:10595 hereditary motor and sensory neuropathy hereditary sensorimotor neuropathy Charcot-Marie-Tooth hereditary neuropathy UMLS:C0007959 NCIT:C75467 NANDO:1200016 MONDO:0015626 ICD9:356.1 MEDGEN:2980 Orphanet:166 CMT MESH:D002607 CMT/HMSN Charcot Marie Tooth muscular atrophy hereditary peripheral neuropathy