Idiopathic non-lupus full-house nephropathy

disorder

SNOMED 1260197005CUI C5680132

Overview

Idiopathic non-lupus full-house nephropathy 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.

Proteinuria

Very frequent (80-99%)HP:0000093

Complement deficiency

Frequent (30-79%)HP:0004431

Decreased serum complement C3 level

Frequent (30-79%)HP:0005421

Decreased serum complement C4 level

Frequent (30-79%)HP:0045042

High blood pressure

Frequent (30-79%)HP:0000822

Nephrosis

Frequent (30-79%)HP:0000100

Renal failure

Frequent (30-79%)HP:0000083

Abnormality of the glomerular mesangium

Occasional (5-29%)HP:0001966

Acute kidney failure

Occasional (5-29%)HP:0001919

C3 nephropathy

Occasional (5-29%)HP:0012576

Glomerulonephritis

Occasional (5-29%)HP:0000099

Increased creatinine

Occasional (5-29%)HP:0003259

Joint inflammation

Occasional (5-29%)HP:0001369

Microhematuria

Occasional (5-29%)HP:0002907

Mouth ulcer

Occasional (5-29%)HP:0000155

Serositis

Occasional (5-29%)HP:0045073

Skin rash

Occasional (5-29%)HP:0000988

Synovitis

Occasional (5-29%)HP:0100769

Brain and/or spinal cord issue

Very rare (1-4%)HP:0000707

Immunological abnormality

Very rare (1-4%)HP:0002715

Related Conditions

Glomerular disease(parent)

Idiopathic disease(parent)

Kidney lesion(parent)

Abnormal renal corpuscle morphology(parent)

Quick Facts

SNOMED CT: 1260197005
UMLS CUI: C5680132
Fully Specified Name: Idiopathic non-lupus full-house nephropathy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 20

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.