has material basis in germline mutation in HK1 motor peripheral neuropathy Charcot-Marie-Tooth disease type 4G https://github.com/monarch-initiative/mondo/issues/4985 https://www.malacards.org/card/neuropathy_hereditary_motor_and_sensory_russe_type MONDO:0011534 Charcot-Marie-Tooth disease type 4G (CMT4G) is a subtype of Charcot-Marie-Tooth disease type 4 characterized by early childhood onset of progressive distal muscle weakness and atrophy, delayed motor development, prominent distal sensory impairment, areflexia, moderately reduced nerve conduction velocities, and foot and hand deformities in Balkan (Russe) Gypsies. HMSNR CMT4G hereditary motor and sensory neuropathy, Russe type UMLS:C1854449 OMIM:605285 neuropathy, hereditary motor and sensory, Russe type Charcot-Marie-Tooth disease type 4 caused by mutation in HK1 HK1 Charcot-Marie-Tooth disease type 4 Orphanet:99953 MESH:C535813 DOID:0110196 GARD:0010132 MEDGEN:343122 SCTID:715799004 icd11.foundation:995395080 disorder of glycolysis Charcot-Marie-Tooth disease type 4