| hereditaire distale motorische neuropathie type 2 (aandoening) | | hereditaire distale motorische neuropathie type 2 | | dSMA2
dHMN2
autosomaal dominante distale spinale spieratrofie type 2
| | Distal hereditary motor neuropathy type 2 | | Autosomal dominant distal spinal muscular atrophy type 2
| | A rare autosomal dominant distal hereditary motor neuropathy with characteristics of onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life. Sensory involvement is typically less pronounced or absent. The severity of the condition is variable and both lower and upper extremities may be involved. |
| | Id | 1230343006 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 139525 |
| 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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