Overview
Methimazole embryofetopathy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Esophageal atresia
Very frequent (80-99%)HP:0002032
Hydramnios
Very frequent (80-99%)HP:0001561
Hypothyroidism
Very frequent (80-99%)HP:0000821
Small for gestational age infant
Very frequent (80-99%)HP:0001511
Tracheoesophageal fistula
Very frequent (80-99%)HP:0002575
Abnormal aortic morphology
Frequent (30-79%)HP:0001679
Abnormality of the thyroid gland
Frequent (30-79%)HP:0000820
Aortic coarctation
Frequent (30-79%)HP:0001680
Choanal atresia
Frequent (30-79%)HP:0000453
Hypospadias
Frequent (30-79%)HP:0000047
Skull defect
Frequent (30-79%)HP:0001362
Urogenital fistula
Frequent (30-79%)HP:0100589
VSD
Frequent (30-79%)HP:0001629
Related Conditions
Quick Facts
- SNOMED CT
- 724144006
- UMLS CUI
- C4510379
- Fully Specified Name
- Embryofetopathy caused by methimazole (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 13
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.