Charcot-Marie-Tooth disease axonal type 2N (DOID:0110177)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2N; autosomal dominant Charcot-Marie-Tooth disease type 2N; Charcot-Marie-Tooth neuropathy axonal type 2N; CMT2N
Alt IDs: OMIM:613287, ICD10CM:G60.0, ORDO:228174
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the AARS gene on chromosome 16q21.