Charcot-Marie-Tooth disease axonal type 2O (DOID:0110175)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2O; autosomal dominant Charcot-Marie-Tooth disease type 2O; Charcot-Marie-Tooth neuropathy axonal type 2O
Alt IDs: OMIM:614228, ICD10CM:G60.0, ORDO:284232
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32.