Charcot-Marie-Tooth disease type 4G (DOID:0110196)
Alliance: disease page
Synonyms: autosomal recessive Charcot-Marie-Tooth disease type 4G; Charcot-Marie-Tooth neuropathy type 4G; CMT4G; hereditary motor and sensory neuropathy Russe type; HMSNR
Alt IDs: OMIM:605285, ICD10CM:G60.0, ORDO:99953
Definition: A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.