amyotrofische laterale sclerose type 1
autosomaal dominante hereditaire aandoening
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autosomaal dominante amyotrofische laterale sclerose type 1 (aandoening)
autosomaal dominante amyotrofische laterale sclerose type 1
autosomaal dominante ALS type 1
Autosomal dominant amyotrophic lateral sclerosis type 1
ALS1 AD - amyotrophic lateral sclerosis type 1 autosomal dominant
Autosomal dominant ALS (amyotrophic lateral sclerosis) type 1
An autosomal dominant hereditary neurodegenerative disease with characteristics of progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. Associated with mutations in the superoxide dismutase-1 gene (SOD1) on chromosome 21q22.
Id1197523001
StatusDefined
Clinical courseprogressief
Associated morphologydegeneratieve afwijking
Finding sitestructuur van systema nervosum
SNOMED CT to ICD-10 extended map
TargetG12.2
RuleTRUE
AdviceALWAYS G12.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified