Charcot-Marie-Tooth disease, axonal type 2W (DOID:0110162)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2W; Charcot-Marie-Tooth neuropathy type 2W; CMT2W
Alt IDs: OMIM:616625
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the HARS gene on chromosome 5q31.