Hereditary motor and sensory neuropathy   398100001

SNOMED CT code


SNOMED code398100001
nameHereditary motor and sensory neuropathy
statusactive
date introduced2003-07-31
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 sitePeripheral nervous system structure   3058005
parentsHereditary 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
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