Conditions / Skin
hypotrichosis 13
info · Skin
A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the KRT71 gene on chromosome 12q13.13.
Signs and symptoms
- Woolly hair
- Sparse eyelashes
- Sparse hair
- Abnormal dental morphology
- Abnormal skin morphology
- Abnormal sweat gland morphology
Also known as: HYPT13; hypotrichosis with woolly hair