Charcot-Marie-Tooth disease axonal type 2T (DOID:0110160)
Alliance: disease page
Synonyms: AR-CMT2T; autosomal recessive axonal Charcot-Marie-Tooth disease type 2T; Charcot-Marie-Tooth neuropathy type 2T; CMT2T
Alt IDs: OMIM:617017, ICD10CM:G60.0, ORDO:443950
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.