Conditions / Syndrome
ectodermal dysplasia 10A
info · Syndrome
A hypohidrotic ectodermal dysplasia that has_material_basis_in heterozygous mutation in the EDAR gene on chromosome 2q13.
Signs and symptoms
- Hypohidrosis
- Sparse eyebrow
- Fine hair
- Microdontia
- Sparse hair
- Dry skin
- Ectodermal dysplasia
- Sparse eyelashes
- Anodontia
- Slow-growing hair
Also known as: ECTD10A; ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant