juveniele amyotrofische laterale sclerose
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juveniele amyotrofische laterale sclerose type 2 (aandoening)
juveniele amyotrofische laterale sclerose type 2
juveniele ALS type 2
Juvenile amyotrophic lateral sclerosis type 2
Juvenile amyotrophic lateral sclerosis due to ALS2 gene mutation
JALS (juvenile amyotrophic lateral sclerosis) type 2
A very rare severe motor neuron disease with manifestation of progressive upper and lower motor neuron degeneration causing facial spasticity, dysarthria, and gait disorders with onset before 25 years of age. Caused by homozygous mutation in the gene encoding alsin ALS2 (2q33-q35).
Id1201947005
StatusPrimitive
Clinical courseprogressief
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