A Charcot-Marie-Tooth disease type 1 that has_material_basis_in duplication of, or mutation in, the gene encoding peripheral myelin protein-22 (PMP22).
synonyms:
ORDO:101081,
CMT1A,
hereditary motor and sensory neuropathy 1A,
118220,
Charcot-Marie-Tooth neuropathy type 1A,
GARD:1245,
ICD10CM:G60.0,
autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A,
