Autosomal dominant multiple pterygium syndrome 771269000
SNOMED CT code
| SNOMED code | 771269000 |
|---|---|
| name | Autosomal dominant multiple pterygium syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Autosomal dominant multiple pterygium syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Has interpretation | Decreased 1250004 |
| Interprets | Range of joint movement 364564000 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Structure of joint region 785818007 |
| Associated morphology | Contracture 57048009 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Congenital webbing 76640006 |
| Finding site | Skin structure 39937001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Autosomal dominant multiple pterygium syndrome 771269000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Multiple pterygium syndrome 205819008 Autosomal dominant multiple pterygium syndrome 771269000 SNOMED CT Concept 138875005 Clinical finding 404684003 Deformity 417893002 Congenital deformity 276655000 Arthrogryposis 111246005 Distal arthrogryposis syndrome 24269006 Autosomal dominant multiple pterygium syndrome 771269000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Inherited arthrogryposis 28204005 Autosomal dominant multiple pterygium syndrome 771269000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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