Related Conditions
Finnish congenital nephrotic syndrome(child)
Familial mesangial sclerosis(child)
Congenital anomaly of the kidney(parent)
Nephrotic syndrome(parent)
Hereditary nephropathy(parent)
Recessive hereditary disorder (autosomal)(parent)
Developmental hereditary disorder(parent)
Genetic disease of glomerulus(parent)
Abnormal renal corpuscle morphology(parent)
Quick Facts
- SNOMED CT
- 48796009
- UMLS CUI
- C3501848
- Fully Specified Name
- Congenital nephrotic 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.