| amyotrofische laterale sclerose type 3 (aandoening) | | amyotrofische laterale sclerose type 3 | | ALS type 3
| | Amyotrophic lateral sclerosis type 3 | | ALS3 - amyotrophic lateral sclerosis type 3
| | A 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 the ALS3 gene on the cytogenetic location 18q21. |
| | Id | 1201950008 | | Status | Primitive |
| 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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