Amyotonia congenita 63135006
SNOMED CT code
| SNOMED code | 63135006 |
|---|---|
| name | Amyotonia congenita |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Amyotonia congenita (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Neuromuscular junction 31627007 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skeletal muscle structure 127954009 |
| 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 Neuropathy 386033004 Neuromuscular junction disorder 128213006 Disorder of neuromuscular transmission 256321009 Amyotonia congenita 63135006 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Myoneural disorder 257277002 Amyotonia congenita 63135006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Amyotonia congenita 63135006 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 Amyotonia congenita 63135006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Amyotonia congenita 63135006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Amyotonia congenita 63135006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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