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hereditaire motorische en sensorische neuropathie type 5 (aandoening)
hereditaire motorische en sensorische neuropathie type 5
HMSN 5
CMT 5
Hereditary motor and sensory neuropathy type 5
Charcot-Marie-Tooth disease, pyramidal features syndrome
Hereditary sensory-motor neuropathy type V
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.
Id771143004
StatusPrimitive
Clinical courseprogressief
referentieset met zeldzame neuromusculaire aandoeningen
DHD Diagnosethesaurus-referentieset
referentieset met complexe 'mapping' naar ICD-10
TargetG60.0
RuleTRUE
AdviceALWAYS G60.0
CorrelationSNOMED CT source code to target map code correlation not specified