Addison's disease

disorder

SNOMED 363732003CUI C0001403

Overview

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

Treatments & Interventions

Dexamethasone acetate

substance

Fludrocortisone

substance

Fludrocortisone acetate

substance

Desoxycorticosterone pivalate

substance

Dexamethasone

substance

Dexamethasone phosphate

substance

Dexamethasone sodium phosphate

substance

Dexamethasone isonicotinate

substance

Signs & Symptoms

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

Hypocortisolism

Always present (100%)HP:0008163

Primary adrenal insufficiency

Always present (100%)HP:0008207

Autoimmunity

Very frequent (80-99%)HP:0002960

Diarrhea

Very frequent (80-99%)HP:0002014

Dyschezia

Very frequent (80-99%)HP:0002019

Hypotension

Very frequent (80-99%)HP:0002615

Increased circulating ACTH level

Very frequent (80-99%)HP:0003154

Melanoderma

Very frequent (80-99%)HP:0000953

Muscle weakness

Very frequent (80-99%)HP:0001324

Nausea and vomiting

Very frequent (80-99%)HP:0002017

Obsessive dieting

Very frequent (80-99%)HP:0002039

Tiredness

Very frequent (80-99%)HP:0012378

Undergrowth

Very frequent (80-99%)HP:0001508

Upset stomach

Very frequent (80-99%)HP:0002027

Weight loss

Very frequent (80-99%)HP:0001824

Anti-21-hydroxylase antibody positivity

Frequent (30-79%)HP:0034071

Anti-P450scc

Frequent (30-79%)HP:0034055

Anti-steroid 17alpha-hydroxylase antibody positivity

Frequent (30-79%)HP:0034061

Decreased urinary potassium

Frequent (30-79%)HP:0012364

Dehydration

Frequent (30-79%)HP:0001944

Elevated heart rate

Frequent (30-79%)HP:0001649

Hyperkalemia

Frequent (30-79%)HP:0002153

Hyperkalemic metabolic acidosis

Frequent (30-79%)HP:0005976

Hyperuricaemia

Frequent (30-79%)HP:0002149

Hypoandrogenism

Frequent (30-79%)HP:0008226

Hyponatremia

Frequent (30-79%)HP:0002902

Increased plasma renin

Frequent (30-79%)HP:0000848

Malaise

Frequent (30-79%)HP:0033834

Mineralocorticoid insufficiency

Frequent (30-79%)HP:0004319

Normocytic anemia

Frequent (30-79%)HP:0001897

Related Conditions

Tuberculous Addison's disease(child)

Addison's disease with adrenoleucodystrophy(child)

Addison's disease due to autoimmunity(child)

Polyglandular autoimmune syndrome, type 1(child)

Adrenal cortical hypofunction(parent)

Quick Facts

SNOMED CT: 363732003
UMLS CUI: C0001403
Fully Specified Name: Addison's disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30
Known Treatments: 8

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.