Charcot-Marie-Tooth disease type 2A2A (DOID:0110155)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2; Charcot-Marie-Tooth neuronal type 2A2; Charcot-Marie-Tooth neuropathy type 2A2; CMT2A2A; hereditary motor and sensory neuropathy IIA2; HMSN2A2; HMSN IIA2
Alt IDs: OMIM:609260, ICD10CM:G60.0, ORDO:99947
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MFN2 gene on chromosome 1p36.22.