TARP syndrome 725911008
SNOMED CT code
| SNOMED code | 725911008 |
|---|---|
| name | TARP syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Pierre Robin sequence, congenital heart defect, talipes syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 TARP syndrome 725911008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 TARP syndrome 725911008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 TARP syndrome 725911008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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