Insulin resistance - type B

disorder

SNOMED 237652003CUI C0342337

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal circulating fatty-acid concentration

Very frequent (80-99%)HP:0004359

Abnormal glucose tolerance

Very frequent (80-99%)HP:0001952

Abnormal oral glucose tolerance

Very frequent (80-99%)HP:0004924

Acanthosis nigricans

Very frequent (80-99%)HP:0000956

Autoimmunity

Very frequent (80-99%)HP:0002960

Body fails to respond to insulin

Very frequent (80-99%)HP:0000855

Decreased plasma Tg levels

Very frequent (80-99%)HP:0012153

Elevated sedimentation rate

Very frequent (80-99%)HP:0003565

Fasting hyperinsulinemia

Very frequent (80-99%)HP:0008283

Hyperglycemia

Very frequent (80-99%)HP:0003074

Hyperinsulinemia

Very frequent (80-99%)HP:0000842

Postprandial hyperglycemia

Very frequent (80-99%)HP:0011998

SLE

Very frequent (80-99%)HP:0002725

Weight loss

Very frequent (80-99%)HP:0001824

Abnormal circulating lipid concentration

Frequent (30-79%)HP:0003119

Abnormality of circulating leptin level

Frequent (30-79%)HP:0004361

Abnormality of habitus

Frequent (30-79%)HP:0004323

Antinuclear antibodies

Frequent (30-79%)HP:0003493

Decreased serum complement factor B

Frequent (30-79%)HP:0005416

Enlarged ovaries

Frequent (30-79%)HP:0100879

Enlarged ovaries with cysts

Frequent (30-79%)HP:0008675

Glucose in urine

Frequent (30-79%)HP:0003076

Hirsutism

Frequent (30-79%)HP:0001007

Increased testosterone

Frequent (30-79%)HP:0030088

Insulin-resistant diabetes

Frequent (30-79%)HP:0000831

Leukopenia

Frequent (30-79%)HP:0001882

Low albumin

Frequent (30-79%)HP:0003073

Nephritis

Frequent (30-79%)HP:0000123

NIDDM

Frequent (30-79%)HP:0005978

Polycystic ovary disease

Frequent (30-79%)HP:0000147

Related Conditions

Autoimmune endocrine disease(parent)

Diabetes mellitus due to genetic defect in insulin action(parent)

Insulin resistance(parent)

Quick Facts

SNOMED CT: 237652003
UMLS CUI: C0342337
Fully Specified Name: Insulin resistance - type B (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.