Juvenile amyotrophic lateral sclerosis type 2 (disorder) | | 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). |
| Id | 1201947005 | Status | Primitive |
ICD-10 complex map reference set | Target | G12.2 | Rule | TRUE | Advice | ALWAYS G12.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | Correlation | SNOMED CT source code to target map code correlation not specified |
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