Neurogenic arthrogryposis multiplex congenita 715316005
SNOMED CT code
| SNOMED code | 715316005 |
|---|---|
| name | Neurogenic arthrogryposis multiplex congenita |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Neurogenic arthrogryposis multiplex congenita (disorder) |
| synonyms | Neurogenic arthrogryposis multiplex congenita |
| attributes - group1 | |
| Associated morphology | Contracture 57048009 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of joint region 785818007 |
| attributes - group4 | |
| Has interpretation | Decreased 1250004 |
| Interprets | Range of joint movement 364564000 |
| attributes - group3 | |
| Due to | Denervation atrophy of muscle 74035001 |
| parents | |
| children | Arthrogryposis with renal dysfunction and cholestasis syndrome 720513002 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Deformity 417893002 Congenital deformity 276655000 Arthrogryposis 111246005 Arthrogryposis multiplex congenita 205402004 Neurogenic arthrogryposis multiplex congenita 715316005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Inherited arthrogryposis 28204005 Neurogenic arthrogryposis multiplex congenita 715316005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Neurogenic arthrogryposis multiplex congenita 715316005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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