hereditary motor and sensory neuropathy https://github.com/monarch-initiative/mondo/issues/9097 icd11.foundation:1538134578 MONDO:0015358 MESH:D015417 NANDO:2200855 MEDGEN:45066 GARD:0012685 ICD10CM:G60.0 Orphanet:140450 HMSN A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-Tooth DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343) UMLS:C0027888 SCTID:398100001 hereditary peripheral neuropathy