ORPHA:701
Alopecia universalis
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal recessive, Multigenic/multifactorial
- Typical age of onset
- All ages
- Estimated prevalence
- 1-5 / 10 000 (Europe)
- Rarity class
- 1-5 / 10 000
ORPHA:701 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Absent eyelashes
- Absent eyebrow
- Patchy alopecia
- Alopecia universalis
- Abnormality of the thyroid gland
- Hypertension