Antenatal multi-minicore disease with arthrogryposis multiplex congenita 1259119003
SNOMED CT code
| SNOMED code | 1259119003 |
|---|---|
| name | Antenatal multi-minicore disease with arthrogryposis multiplex congenita |
| status | active |
| date introduced | 2022-12-31 |
| fully specified name(s) | Antenatal multi-minicore disease with arthrogryposis multiplex congenita (disorder) |
| synonyms | Antenatal multi-minicore disease with arthrogryposis multiplex congenita |
| attributes - group3 | |
| Interprets | Range of joint movement 364564000 |
| Has interpretation | Decreased 1250004 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skeletal muscle structure 127954009 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of joint region 785818007 |
| Associated morphology | Contracture 57048009 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Deformity 417893002 Congenital deformity 276655000 Arthrogryposis 111246005 Arthrogryposis multiplex congenita 205402004 Antenatal multi-minicore disease with arthrogryposis multiplex congenita 1259119003 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Congenital anomaly of skeletal muscle 89886004 Multi-core congenital myopathy 55133004 Antenatal multi-minicore disease with arthrogryposis multiplex congenita 1259119003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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