SNOMED CT

Last uploaded: January 16, 2025
Id http://purl.bioontology.org/ontology/SNOMEDCT/1172690003
http://purl.bioontology.org/ontology/SNOMEDCT/1172690003
Preferred Name

Propylthiouracil embryofetopathy

Definitions
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).
Synonyms
Disorder of fetus caused by propylthiouracil (disorder)
Disorder of fetus caused by propylthiouracil
Type http://www.w3.org/2002/07/owl#Class
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