Overview
Fetal indomethacin syndrome 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.
Kidney disease
Very frequent (80-99%)HP:0000112
Premature birth
Very frequent (80-99%)HP:0001622
Renal failure
Very frequent (80-99%)HP:0000083
Respiratory function loss
Very frequent (80-99%)HP:0002093
Atria septal defect
Occasional (5-29%)HP:0001631
Blood coagulation disorder
Occasional (5-29%)HP:0001928
Disease of the heart muscle
Occasional (5-29%)HP:0001638
Hydrops fetalis
Occasional (5-29%)HP:0001789
Morphologic abnormality of the renal tubules
Occasional (5-29%)HP:0000091
Multicystic kidney dysplasia
Occasional (5-29%)HP:0000003
Oligohydramnios
Occasional (5-29%)HP:0001562
VSD
Occasional (5-29%)HP:0001629
Related Conditions
Quick Facts
- SNOMED CT
- 715430001
- UMLS CUI
- C4275138
- Fully Specified Name
- Embryofetopathy caused by indomethacin (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 12
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.