Overview
Finnish congenital nephrotic 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.
Anasarca
Always present (100%)HP:0012050
Elevated total cholesterol
Always present (100%)HP:0003124
Hypoalbuminaemia
Always present (100%)HP:0003073
Hypoproteinemia
Always present (100%)HP:0003075
Delayed eruption of permanent teeth
Very frequent (80-99%)HP:0000696
Elevated amniotic fluid alpha-fetoglobulin
Very frequent (80-99%)HP:0004639
Morphologic abnormality of the renal tubules
Very frequent (80-99%)HP:0000091
Nephrosis
Very frequent (80-99%)HP:0000100
Proteinuria
Very frequent (80-99%)HP:0000093
End-stage renal disease
Frequent (30-79%)HP:0003774
Belly bloating
HP:0003270
Birth weight less than 10th percentile
HP:0001518
Congenital nephrosis
HP:0008677
Diffuse mesangial sclerosis glomerulopathy
HP:0001967
Edema
HP:0000969
Gastro-esophageal reflux
HP:0002020
Glomerulosclerosis
HP:0000096
Growth deficiency
HP:0001510
Hyperlipidemia
HP:0003077
Hypothyroidism
HP:0000821
Infantile hypertrophic pyloric stenosis
HP:0002021
Renal failure in adulthood
HP:0000083
Renal tubular cell atrophy
HP:0000092
Respiratory distress, neonatal
HP:0002643
Susceptibility to infection
HP:0002719
Related Conditions
Quick Facts
- SNOMED CT
- 197601003
- UMLS CUI
- C0403399
- Fully Specified Name
- Finnish congenital nephrotic syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 25
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.