Overview
Congenital malformation syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Multiple system malformation syndrome(child)
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance(child)
Congenital malformation syndromes associated with short stature(child)
Facial milia, lobate tongue, lingual and labial frenula syndrome(child)
Malformation sequence(child)
CPLS - cleft palate-lateral synechia syndrome(child)
Cardio-acral-facial syndrome(child)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma(child)
Cardio-facio-cutaneous syndrome(child)
First and second branchial arch syndrome(child)
X-linked intellectual disability Pai type(child)
X-linked intellectual disability Miles Carpenter type(child)
X-linked intellectual disability Armfield type(child)
X-linked intellectual disability Abidi type(child)
Gorlin-Chaudhry-Moss syndrome(child)
Methimazole embryofetopathy(child)
Fetal iodine syndrome(child)
Congenital malformation caused by cytotoxic agents(child)
Embryopathy caused by mycophenolate mofetil(child)
Fetal indomethacin syndrome(child)
Quick Facts
- SNOMED CT
- 400038003
- UMLS CUI
- C1302790
- Fully Specified Name
- Congenital malformation syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.