Conditions / Skin
hypotrichosis 11
info · Skin
A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the SNRPE gene on chromosome 1q32.1.
Signs and symptoms
- Sparse hair
- Absent axillary hair
- Aplasia/Hypoplasia of the eyebrow
- Sparse or absent eyelashes
- Alopecia universalis
Also known as: HYPT11