Juvenile amyotrophic lateral sclerosis type 5 (disorder) | | Juvenile amyotrophic lateral sclerosis type 5 | | ALS5 - amyotrophic lateral sclerosis type 5
| | 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. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the spatacsin gene (SPG11) on chromosome 15q21. |
| Id | 1201961000 | 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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