| autosomaal recessieve amyotrofische laterale sclerose type 1 (aandoening) | | autosomaal recessieve amyotrofische laterale sclerose type 1 | | autosomaal recessieve ALS type 1
| | Autosomal recessive amyotrophic lateral sclerosis type 1 | | ALS1 AR - amyotrophic lateral sclerosis type 1 autosomal recessive
Autosomal recessive ALS (amyotrophic lateral sclerosis) type 1
| | An autosomal recessive 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 | 1197524007 | | Status | Defined |
| SNOMED CT to ICD-10 extended map | | 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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