Autosomal dominant omodysplasia 725165009
SNOMED CT code
| SNOMED code | 725165009 |
|---|---|
| name | Autosomal dominant omodysplasia |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Autosomal dominant omodysplasia (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| Finding site | Bone structure of upper limb 371195002 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Arm length 249748003 |
| 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 omodysplasia 725165009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Finding of upper limb 116307009 Finding of bone of upper limb 298756009 Autosomal dominant omodysplasia 725165009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Finding of upper limb 116307009 Disorder of upper limb 118947000 Congenital anomaly of upper limb 66510004 Autosomal dominant omodysplasia 725165009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Omodysplasia 725164008 Autosomal dominant omodysplasia 725165009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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