Hereditary motor neuron disease
Lower motor neuron disease
||
Spinal muscular atrophy (disorder)
Spinal muscular atrophy
SMA - Spinal muscular atrophy
spinale spieratrofie
spinale musculaire atrofie
SMA
spinale musculaire atrofie
SMA
Spinale musculaire atrofie (SMA) zijn spierziekten waarbij het ziekteproces in het ruggenmerg plaatsvindt (spinaal), waardoor de spieren (musculair) uiteindelijk dunner en slapper worden (atrofie). Dit leidt tot spierzwakte en verlammingen.
Id5262007
StatusPrimitive
Finding siteStructure of nervous system
PALGA thesaurus simple reference set for pathology
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG12.9
RuleTRUE
AdviceALWAYS G12.9
CorrelationSNOMED CT source code to target map code correlation not specified
|
Adult spinal muscular atrophy
Autosomal dominant adult-onset proximal spinal muscular atrophy
Autosomal dominant hereditary spinal muscular atrophy6
Bulbospinal neuronopathy
Distal spinal muscular atrophy8
Facioscapulohumeral spinal muscular atrophy1
Kugelberg-Welander disease
Lower motor neuron syndrome with late-adult onset
Oculopharyngeal spinal muscular atrophy
Progressive bulbar palsy of childhood
Scapulohumeral spinal muscular atrophy
Scapuloperoneal spinal muscular atrophy
Spinal atrophy, ophthalmoplegia, pyramidal syndrome
Spinal muscular atrophy with lower extremity predominance
Spinal muscular atrophy with progressive myoclonic epilepsy
Spinal muscular atrophy with progressive myoclonic epilepsy
Spinal muscular atrophy, type II
Werdnig-Hoffmann disease
Werdnig-Hoffmann disease
X-linked distal arthrogryposis multiplex congenita