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Hereditary motor and sensory neuropathy type 5 (disorder)
Hereditary motor and sensory neuropathy type 5
Hereditary sensory-motor neuropathy type V
Charcot-Marie-Tooth disease, pyramidal features syndrome
A rare axonal hereditary motor and sensory neuropathy with characteristics of slowly progressive distal muscle weakness and atrophy with or without sensory loss resulting in difficulty in walking, foot drop and pes cavus, that may be associated with pyramidal signs (extensor plantar responses, mild increase in tone, brisk tendon reflexes), muscle cramps, pain and spasticity.
hereditaire motorische en sensorische neuropathie type 5
HMSN 5
CMT 5
Id771143004
StatusPrimitive
Clinical courseProgressive
Dutch rare neuromuscular disorders simple 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