1172690003: Disorder of fetus caused by propylthiouracil (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Fetal finding\Fetal disorder\...
• \Disorder of fetal structure\Propylthiouracil embryofetopathy
• \Fetus with drug damage\Propylthiouracil embryofetopathy
• \Disease\Disorder of fetus or newborn\Fetal disorder\Disorder of fetal structure\Propylthiouracil embryofetopathy
• \Disease\Disorder of fetus or newborn\Fetal disorder\Fetus with drug damage\Propylthiouracil embryofetopathy
• \Disease\Developmental disorder\Disorder of fetal structure\Propylthiouracil embryofetopathy

Status: current, Defined. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4635381016	Disorder of fetus caused by propylthiouracil (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4635382011	Disorder of fetus caused by propylthiouracil	en	Synonym	Active	Case insensitive	SNOMED CT core
4635384012	Propylthiouracil embryofetopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
4746771000168117	Propylthiouracil embryofoetopathy	en	Synonym	Active	Case insensitive	SNOMED Clinical Terms Australian extension
4635383018	A rare teratologic disease with characteristics of variable congenital anomalies resulting from maternal treatment and prenatal exposure to propylthiouracil. Anomalies frequently encountered include ear malformations (e.g. accessory auricle, preauricular sinus/fistula/cyst), urinary system malformations (e.g. isolated unilateral kidney, congenital hydronephrosis), gastrointestinal anomalies (e.g. congenital bands with intestinal malrotation) and cardiac defects (e.g. situs inversus dextrocardia, cardiac outflow tract defects).	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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