Overview
Congenital hamartoma is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Peutz-Jeghers syndrome(child)
Congenital hamartoma of skin(child)
Gardner syndrome(child)
Lhermitte-Duclos disease(child)
Perlman syndrome(child)
Congenital rhabdomyomatous mesenchymal hamartoma(child)
Fibrous skin tumor of tuberous sclerosis(child)
Pulmonary tuberous sclerosis(child)
Congenital hamartoma of iris(child)
Cystic hamartoma of lung and kidney(child)
Hamartoma(parent)
Congenital disease(parent)
Quick Facts
- SNOMED CT
- 399960008
- UMLS CUI
- C1302749
- Fully Specified Name
- Congenital hamartoma (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.