KIN - karyomegalic interstitial nephritis

disorder

SNOMED 782738008CUI C3553774

Overview

KIN - karyomegalic interstitial nephritis 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.

Nephronophthisis

Always present (100%)HP:0000090

Renal interstitial fibrosis

Always present (100%)HP:0032948

Renal tubular cyst

Always present (100%)HP:0041050

Tubulointerstitial nephritis

Always present (100%)HP:0001970

Elevated serum transaminases

Frequent (30-79%)HP:0002910

Glucose in urine

Frequent (30-79%)HP:0003076

Proteinuria

Frequent (30-79%)HP:0000093

Blood in urine

Occasional (5-29%)HP:0000790

End-stage renal disease

HP:0003774

Increased blood urea nitrogen

HP:0003138

Increased creatinine

HP:0003259

Related Conditions

Connective tissue hereditary disorder(parent)

Recessive hereditary disorder (autosomal)(parent)

Renal interstitial fibrosis(parent)

Hereditary nephropathy(parent)

Chronic interstitial nephritis(parent)

Quick Facts

SNOMED CT: 782738008
UMLS CUI: C3553774
Fully Specified Name: Karyomegalic interstitial nephritis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.