Hereditary peripheral neuropathy
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Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy
Hereditary sensory-motor neuropathy
Hereditary sensory and motor neuropathy
HSMN
HSMN - Hereditary sensory and motor neuropathy
CMT - Charcot-Marie-Tooth disease
HMSN - Hereditary motor and sensory neuropathy
Hereditary sensorimotor neuropathy
HMSN
hereditaire motorische en sensorische neuropathie
HMSN
ziekte van Charcot-Marie-Tooth
CMT
HMSN
Hereditaire motorische en sensorische neuropathieën (HMSN) zijn zenuwaandoeningen (neuropathieën), die erfelijk (hereditair) zijn en gevolgen hebben voor het kunnen voelen (sensorisch) en bewegen (motorisch).
Id398100001
StatusPrimitive
Finding sitePeripheral nervous system structure
PALGA thesaurus simple reference set for pathology
Dutch rare neuromuscular disorders simple reference set
General Practice / Family Practice reference set
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG60.0
RuleTRUE
AdviceALWAYS G60.0
CorrelationSNOMED CT source code to target map code correlation not specified
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Andermann syndrome
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
Autosomal dominant slowed nerve conduction velocity
Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy
Charcot-Marie-Tooth disease type 412
Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
Charcot-Marie-Tooth disease, type II4
Digital extensor muscle aplasia with polyneuropathy
Déjérine-Sottas disease
Hereditary motor and sensory neuropathy Okinawa type
Hereditary motor and sensory neuropathy type 5
Hereditary motor and sensory neuropathy with acrodystrophy
Hereditary motor and sensory neuropathy with optic atrophy
Hereditary motor and sensory neuropathy with retinitis pigmentosa
Hereditary sensorimotor neuropathy with hyperelastic skin
Hereditary sensory neuropathy3
Hereditary sensory-motor neuropathy, type I7
Hereditary thermosensitive neuropathy
HSMN IV2
Microcephalus, complex motor and sensory axonal neuropathy syndrome
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome
PMP22-RAI1 contiguous gene duplication syndrome
Roussy-Lévy syndrome
Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
X-linked hereditary motor and sensory neuropathy6