Propylthiouracil embryofetopathy 1172690003
SNOMED CT code
| SNOMED code | 1172690003 |
|---|---|
| name | Propylthiouracil embryofetopathy |
| status | active |
| date introduced | 2021-09-30 |
| fully specified name(s) | Disorder of fetus caused by propylthiouracil (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Fetal period 303112003 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Causative agent | Propylthiouracil 387203007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Fetal finding 106112009 Fetal disorder 70591005 Fetus with drug damage 199547006 Propylthiouracil embryofetopathy 1172690003 SNOMED CT Concept 138875005 Clinical finding 404684003 Fetal finding 106112009 Fetal disorder 70591005 Fetal disorder caused by chemicals 363127005 Propylthiouracil embryofetopathy 1172690003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of fetal structure 609520005 Propylthiouracil embryofetopathy 1172690003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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