Overview
Polyglandular autoimmune syndrome, type 2 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.
Brachydactyly
Always present (100%)HP:0001156
Partial syndactyly
Always present (100%)HP:0006101
Syndactyly of feet
Always present (100%)HP:0001770
Abnormality of the skull bones
Very frequent (80-99%)HP:0000929
Accelerated linear growth
Very frequent (80-99%)HP:0000098
Addison's disease
Very frequent (80-99%)HP:0008207
Asymmetry of the posterior cranium
Very frequent (80-99%)HP:0001357
Big calvaria
Very frequent (80-99%)HP:0000256
Coeliac disease
Very frequent (80-99%)HP:0002608
Craniosyostosis
Very frequent (80-99%)HP:0001363
Cryptorchidism
Very frequent (80-99%)HP:0000028
Curvature of little finger
Very frequent (80-99%)HP:0004209
Graves disease
Very frequent (80-99%)HP:0100647
Hashimoto's thyroiditis
Very frequent (80-99%)HP:0000872
Hypogenitalism
Very frequent (80-99%)HP:0003241
Hypoplastic hands
Very frequent (80-99%)HP:0004279
Increased distance between eyes
Very frequent (80-99%)HP:0000316
Mental deficiency
Very frequent (80-99%)HP:0001249
Obesity
Very frequent (80-99%)HP:0001513
Oxycephaly
Very frequent (80-99%)HP:0000263
Palpebronasal fold
Very frequent (80-99%)HP:0000286
Polydactyly
Very frequent (80-99%)HP:0010442
Prominent frontal suture
Very frequent (80-99%)HP:0005487
Syndactyly
Very frequent (80-99%)HP:0001159
Thin face
Very frequent (80-99%)HP:0000275
Thyroid disease
Very frequent (80-99%)HP:0000820
Type I diabetes mellitus
Very frequent (80-99%)HP:0100651
Abnormal reproductive system morphology
Frequent (30-79%)HP:0012243
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Anti-steroid 17alpha-hydroxylase antibody positivity
Frequent (30-79%)HP:0034061
Related Conditions
Quick Facts
- SNOMED CT
- 83728000
- UMLS CUI
- C0085860
- Fully Specified Name
- Polyglandular autoimmune syndrome, type 2 (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.