Hereditary motor and sensory neuropathy 398100001 SNOMED CT code SNOMED code 398100001 name Hereditary motor and sensory neuropathy status active date introduced 2003-07-31 fully specified name(s) Hereditary motor and sensory neuropathy (disorder) synonyms Hereditary motor and sensory neuropathy Hereditary sensory and motor neuropathy Hereditary sensory-motor neuropathy Hereditary sensorimotor neuropathy CMT - Charcot-Marie-Tooth disease HMSN - hereditary motor and sensory neuropathy HSMN - hereditary sensory and motor neuropathy attributes - group1 Finding site Peripheral nervous system structure 3058005 parents Hereditary peripheral neuropathy 65017003 children Andermann syndrome 702439002 Autosomal dominant intermediate Charcot-Marie-Tooth disease type A 765744006 Autosomal dominant intermediate Charcot-Marie-Tooth disease type B 765745007 Autosomal dominant intermediate Charcot-Marie-Tooth disease type C 765746008 Autosomal dominant intermediate Charcot-Marie-Tooth disease type D 765747004 Autosomal dominant intermediate Charcot-Marie-Tooth disease type E 722294004 Autosomal dominant intermediate Charcot-Marie-Tooth disease type F 770759001 Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain 778003000 Autosomal dominant slowed nerve conduction velocity 764854006 Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect 1187619001 Autosomal recessive intermediate Charcot-Marie-Tooth disease type A 773308001 Autosomal recessive intermediate Charcot-Marie-Tooth disease type B 773330000 Autosomal recessive intermediate Charcot-Marie-Tooth disease type C 773414009 Autosomal recessive intermediate Charcot-Marie-Tooth disease type D 1187567002 Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy 1222704008 Charcot-Marie-Tooth disease type 4 715795005 Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome 763136000 Charcot-Marie-Tooth disease, type II 398187000 Charcot-Marie-Tooth Neuropathy Type 4 67661000119100 Congenital axonal neuropathy with encephalopathy 1237626001 Digital extensor muscle aplasia with polyneuropathy 771261002 Déjérine-Sottas disease 111499002 Hereditary motor and sensory neuropathy Okinawa type 715665006 Hereditary motor and sensory neuropathy type 5 771143004 Hereditary motor and sensory neuropathy with acrodystrophy 771144005 Hereditary motor and sensory neuropathy with optic atrophy 128203003 Hereditary motor and sensory neuropathy with retinitis pigmentosa 128204009 Hereditary sensorimotor neuropathy with hyperelastic skin 782881002 Hereditary sensory neuropathy 11442006 Hereditary sensory-motor neuropathy, type I 398040009 Hereditary thermosensitive neuropathy 715645004 Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000 Microcephalus, complex motor and sensory axonal neuropathy syndrome 763798008 Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome 1222646006 Phytanic acid storage disease 25362006 PMP22-RAI1 contiguous gene duplication syndrome 1172899000 Roussy-Lévy syndrome 45853006 Severe early-onset axonal neuropathy due to mitofusin 2 deficiency 766977007 X-linked hereditary motor and sensory neuropathy 230552007 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hereditary peripheral neuropathy 65017003 Hereditary motor and sensory neuropathy 398100001 ancestors sorted most to least specific
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