Autosomal dominant congenital benign spinal muscular atrophy 763067000
SNOMED CT code
| SNOMED code | 763067000 |
|---|---|
| name | Autosomal dominant congenital benign spinal muscular atrophy |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Autosomal dominant congenital benign spinal muscular atrophy (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Peripheral nervous system structure 3058005 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Nerve structure 3057000 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Autosomal dominant distal hereditary motor neuropathy 1156837002 Autosomal dominant congenital benign spinal muscular atrophy 763067000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hereditary motor neuron disease 49793008 Spinal muscular atrophy 5262007 Distal spinal muscular atrophy 230247001 Autosomal dominant congenital benign spinal muscular atrophy 763067000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Autosomal dominant congenital benign spinal muscular atrophy 763067000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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