Thomas syndrome 716740009
SNOMED CT code
| SNOMED code | 716740009 | ||
|---|---|---|---|
| name | Thomas syndrome | ||
| status | active | ||
| date introduced | 2016-07-31 | ||
| fully specified name(s) | Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | ||
| synonyms |
| ||
| attributes - group1 | |||
| Pathological process | Pathological developmental process 308490002 | ||
| Associated morphology | Morphologically abnormal structure 49755003 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Heart structure 80891009 | ||
| attributes - group2 | |||
| Associated morphology | Morphologically abnormal structure 49755003 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Face structure 89545001 | ||
| parents | |||
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding by site 118234003 Cardiovascular finding 106063007 Cardiac finding 301095005 Heart disease 56265001 Structural disorder of heart 128599005 Congenital heart disease 13213009 Thomas syndrome 716740009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Thomas syndrome 716740009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Thomas syndrome 716740009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Thomas syndrome 716740009 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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