Late-onset isolated ACTH deficiency

disorder

SNOMED 773989002CUI C4751433

Overview

Late-onset isolated ACTH deficiency 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.

ACTH deficiency

Always present (100%)HP:0011748

ACTH deficient adrenal insufficiency

Always present (100%)HP:0011735

Plasma cortisol low

Always present (100%)HP:0008163

Autoimmune disorder

Very frequent (80-99%)HP:0002960

Decreased circulating ACTH concentration

Very frequent (80-99%)HP:0002920

Diarrhea

Very frequent (80-99%)HP:0002014

Dyschezia

Very frequent (80-99%)HP:0002019

Gastro pain

Very frequent (80-99%)HP:0002027

Hypotension

Very frequent (80-99%)HP:0002615

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

Torpor

Very frequent (80-99%)HP:0001254

Undergrowth

Very frequent (80-99%)HP:0001508

Weight loss

Very frequent (80-99%)HP:0001824

Graves disease

Frequent (30-79%)HP:0100647

Hashimoto's thyroiditis

Frequent (30-79%)HP:0000872

Hyperuricaemia

Frequent (30-79%)HP:0002149

Hyponatremia

Frequent (30-79%)HP:0002902

Macrocytic anemia

Frequent (30-79%)HP:0001972

Mild fever

Frequent (30-79%)HP:0011134

Normocytic anemia

Frequent (30-79%)HP:0001897

Premature menopause

Frequent (30-79%)HP:0008209

Type I diabetes mellitus

Frequent (30-79%)HP:0100651

Arthralgias

Occasional (5-29%)HP:0002829

Blotchy loss of skin colour

Occasional (5-29%)HP:0001045

Coeliac disease

Occasional (5-29%)HP:0002608

Decrease in blood pressure upon standing up

Occasional (5-29%)HP:0001278

Eosinophilia

Occasional (5-29%)HP:0001880

Related Conditions

Secondary hypoadrenalism(parent)

Quick Facts

SNOMED CT: 773989002
UMLS CUI: C4751433
Fully Specified Name: Late-onset isolated adrenocorticotropic hormone deficiency (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.