Autoimmune polyendocrine syndrome type 4

disorder

SNOMED 449730005CUI C3266026

Overview

Autoimmune polyendocrine syndrome type 4 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.

Autoimmunity

Always present (100%)HP:0002960

Autoimmune antibody positivity

Frequent (30-79%)HP:0030057

Chronic atrophic gastritis

Frequent (30-79%)HP:0002582

Coeliac disease

Frequent (30-79%)HP:0002608

Macrocytic anemia

Frequent (30-79%)HP:0001972

Type I diabetes mellitus

Frequent (30-79%)HP:0100651

Anterior pituitary dysgenesis

Occasional (5-29%)HP:0010625

Blotchy loss of skin colour

Occasional (5-29%)HP:0001045

Decreased serum immunoglobulin

Occasional (5-29%)HP:0004313

Hair loss

Occasional (5-29%)HP:0001596

Leukopenia

Occasional (5-29%)HP:0001882

Primary biliary cirrhosis

Occasional (5-29%)HP:0002613

Abnormal lung parenchyma morphology

Very rare (1-4%)HP:0006530

Antiphospholipid antibodies

Very rare (1-4%)HP:0003613

Aplasia/Hypoplasia of the spleen

Very rare (1-4%)HP:0010451

Dry eye syndrome

Very rare (1-4%)HP:0001097

Hepatitis

Very rare (1-4%)HP:0012115

Idiopathic thrombocytopenia

Very rare (1-4%)HP:0001973

Iridocyclitis

Very rare (1-4%)HP:0001094

Neurohypophyseal diabetes insipidus

Very rare (1-4%)HP:0000863

Non-caseating epithelioid cell granulomatosis

Very rare (1-4%)HP:0012220

Osteopenia

Very rare (1-4%)HP:0000938

Primary hypogonadism

Very rare (1-4%)HP:0000815

Rheumatoid arthritis

Very rare (1-4%)HP:0001370

Skin bullae

Very rare (1-4%)HP:0008066

Thymoma

Very rare (1-4%)HP:0100522

Tubulointerstitial nephritis

Very rare (1-4%)HP:0001970

Xerostomia

Very rare (1-4%)HP:0000217

Related Conditions

Autoimmune polyendocrinopathy(parent)

Quick Facts

SNOMED CT: 449730005
UMLS CUI: C3266026
Fully Specified Name: Autoimmune polyendocrine syndrome type 4 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 28

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.