Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Absent eyelashes
Very frequent (80-99%)HP:0000561
Agenesis of eyebrows
Very frequent (80-99%)HP:0002223
Alopecia areata
Very frequent (80-99%)HP:0002232
Abnormal circulating lipid concentration
Occasional (5-29%)HP:0003119
Abnormal nail morphology
Occasional (5-29%)HP:0001597
Abnormality of the thyroid gland
Occasional (5-29%)HP:0000820
Autoimmunity
Occasional (5-29%)HP:0002960
High blood pressure
Occasional (5-29%)HP:0000822
Infantile eczema
Occasional (5-29%)HP:0001047
Blotchy loss of skin colour
Very rare (1-4%)HP:0001045
Psoriasiform dermatitis
Very rare (1-4%)HP:0003765
Type I diabetes mellitus
Very rare (1-4%)HP:0100651
Alopecia universalis
HP:0002289
Nail pitting
HP:0001803
Total alopecia
HP:0007418
Trachyonychia
HP:0030804
Related Conditions
Quick Facts
- SNOMED CT
- 86166000
- UMLS CUI
- C0263505
- Fully Specified Name
- Alopecia universalis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 16
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.