propylthiouracil embryofetopathy
Findings
No curated finding names propylthiouracil embryofetopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Propylthiouracil embryofetopathy is a rare teratologic disease characterized by 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).
Definition from the Mondo Disease Ontology (MONDO:0044619), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
3 names
Resolves to: propylthiouracil embryofetopathy
- Also called
- propylthiouracil embryopathyPTU embryofetopathyPTU embryopathy