Immunoglobulin G4 related kidney disease

disorder

SNOMED 1187507004CUI C5392056

Overview

Immunoglobulin G4 related kidney disease 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.

Increased circulating IgG4 level

Very frequent (80-99%)HP:0032300

Increased total IgG in blood

Very frequent (80-99%)HP:0003237

Tubulointerstitial nephritis

Very frequent (80-99%)HP:0001970

Acute kidney failure

Frequent (30-79%)HP:0001919

Antinuclear antibodies

Frequent (30-79%)HP:0003493

CKD

Frequent (30-79%)HP:0012622

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 urine occult blood

Frequent (30-79%)HP:0000790

Increased circulating IgG1 level

Frequent (30-79%)HP:0032298

Increased creatinine

Frequent (30-79%)HP:0003259

Proteinuria

Frequent (30-79%)HP:0000093

Renal failure

Frequent (30-79%)HP:0000083

Renal interstitial immunoglobulin deposits

Frequent (30-79%)HP:0032616

Rheumatoid factor positive

Frequent (30-79%)HP:0002923

Abnormal aortic morphology

Occasional (5-29%)HP:0001679

Abnormal breast morphology

Occasional (5-29%)HP:0031093

Abnormal ureter morphology

Occasional (5-29%)HP:0025633

Abnormality of the anterior pituitary

Occasional (5-29%)HP:0011747

Abnormality of the mediastinum

Occasional (5-29%)HP:0045026

Abnormality of the mesentery

Occasional (5-29%)HP:0100016

Albuminuria

Occasional (5-29%)HP:0012592

Cystitis of the urinary bladder

Occasional (5-29%)HP:0100577

Dacrocystitis

Occasional (5-29%)HP:0000620

Decreased retinol-binding protein level

Occasional (5-29%)HP:0031032

Enlarged kidney

Occasional (5-29%)HP:0000105

Eosinophilia

Occasional (5-29%)HP:0001880

Fibrous cholangitis

Occasional (5-29%)HP:0030991

Gallbladder inflammation

Occasional (5-29%)HP:0001082

Related Conditions

IgG4 related disease(parent)

Autoimmune connective tissue disorder(parent)

Tubulo-interstitial nephritis(parent)

Quick Facts

SNOMED CT: 1187507004
UMLS CUI: C5392056
Fully Specified Name: Immunoglobulin G4 related kidney disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.