A rare hereditary motor and sensory neuropathy disorder with characteristics of the typical CMT phenotype (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante type F
SNOMEDCT-BE (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend / 770759001
SNOMEDCT-BE (disorder) / 770759001
