Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
MPGN
Very frequent (80-99%)HP:0000793
C3 nephritic factor positivity
Frequent (30-79%)HP:0030888
CKD
Frequent (30-79%)HP:0012622
Decreased serum complement C3 level
Frequent (30-79%)HP:0005421
High blood pressure
Frequent (30-79%)HP:0000822
Membranoproliferative glomerulonephritis type II
Frequent (30-79%)HP:0004746
Microhematuria
Frequent (30-79%)HP:0002907
Nephrosis
Frequent (30-79%)HP:0000100
Proteinuria
Frequent (30-79%)HP:0000093
Renal failure in adulthood
Frequent (30-79%)HP:0000083
Acute kidney failure
Occasional (5-29%)HP:0001919
End-stage renal disease
Occasional (5-29%)HP:0003774
Hypoalbuminaemia
Occasional (5-29%)HP:0003073
Abnormal thrombosis
Very rare (1-4%)HP:0001977
Drusen
Very rare (1-4%)HP:0011510
Myocardial infarction
Very rare (1-4%)HP:0001658
Related Conditions
Mesangiocapillary glomerulonephritis type III(child)
Mesangiocapillary glomerulonephritis type IV(child)
Mesangiocapillary glomerulonephritis, type I(child)
Focal membranoproliferative glomerulonephritis(child)
Complement component 4 glomerulopathy(child)
C3 (complement component 3) glomerulopathy(child)
PGN - Chronic mesangial proliferative glomerulonephritis(parent)
Quick Facts
- SNOMED CT
- 80321008
- UMLS CUI
- C0017662
- Fully Specified Name
- Mesangiocapillary glomerulonephritis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 16
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.