A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante B
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m / 765745007
SNOMEDCT-BE (disorder) / 765745007