A subtype of Autosomal dominant Charcot-Marie-Tooth disease type 2 with the childhood onset of distal weakness and areflexia (with earlier and more severe involvement of the lower extremities), reduced sensory modalities (primarily pain and temperatu
maladie de Charcot-Marie-Tooth autosomique dominante type 2A2
SNOMEDCT-CA (with earlier and more severe involvement of the lower extremities), reduced sensory modalities (primarily pain and temperatu / 764850002
SNOMEDCT-CA (trouble) / 764850002