Familial visceral amyloidosis, Ostertag type

disorder

SNOMED 66451004CUI C0268389

Overview

Familial visceral amyloidosis, Ostertag type 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.

Renal amyloidosis

Always present (100%)HP:0001917

Proteinuria

Very frequent (80-99%)HP:0000093

Renal interstitial amyloidosis

Very frequent (80-99%)HP:0032613

Abnormal urinary electrolyte concentration

Frequent (30-79%)HP:0012591

Decreased glomerular filtration rate

Frequent (30-79%)HP:0012213

Digestive system disease

Frequent (30-79%)HP:0011024

High blood pressure

Frequent (30-79%)HP:0000822

Increased creatinine

Frequent (30-79%)HP:0003259

Renal failure

Frequent (30-79%)HP:0000083

Tubulointerstitial nephritis

Frequent (30-79%)HP:0001970

Abdominal discomfort

Occasional (5-29%)HP:0002027

Abnormal lymph node histology

Occasional (5-29%)HP:0002733

Bowel obstruction

Occasional (5-29%)HP:0005214

Chronic heart failure

Occasional (5-29%)HP:0001635

Decreased circulating apolipoprotein A-I concentration

Occasional (5-29%)HP:0031799

Decreased HDL cholesterol concentration

Occasional (5-29%)HP:0003233

Diarrhea

Occasional (5-29%)HP:0002014

Dyspepsia

Occasional (5-29%)HP:0410281

Elevated sedimentation rate

Occasional (5-29%)HP:0003565

Enlarged liver

Occasional (5-29%)HP:0002240

Gastroesophageal reflux disease

Occasional (5-29%)HP:0002020

Gastrointestinal haemorrhage

Occasional (5-29%)HP:0002239

Hepatosplenomegaly

Occasional (5-29%)HP:0001433

Intestinal perforation

Occasional (5-29%)HP:0031368

Liver dysfunction, mild

Occasional (5-29%)HP:0001410

Low number of red blood cells or haemoglobin

Occasional (5-29%)HP:0001903

Lymph node hyperplasia

Occasional (5-29%)HP:0002716

Myopathy

Occasional (5-29%)HP:0003198

Nausea

Occasional (5-29%)HP:0002018

Nephrosis

Occasional (5-29%)HP:0000100

Related Conditions

Amyloid nephropathy(parent)

Familial non-neuropathic amyloidosis(parent)

Quick Facts

SNOMED CT: 66451004
UMLS CUI: C0268389
Fully Specified Name: Familial visceral amyloidosis, Ostertag type (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.