Charcot-Marie-Tooth disease type 2B2 (DOID:0110179)
Alliance: disease page
Synonyms: AR-CMT2B2; ARCMT2B; autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2; Autosomal recessive axonal CMT4C3; Charcot-Marie-Tooth disease neuronal type 2B2; Charcot-Marie-Tooth neuropathy type 2B2; CMT2B2
Alt IDs: OMIM:605589, ICD10CM:G60.0, MESH:C537991, ORDO:101101
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous mutation in the MED25 gene.