Autosomal dominant amyotrophic lateral sclerosis type 1 (disorder) | | 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. |
| Id | 1197523001 | Status | Defined |
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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