1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0111342 | dermatopathia pigmentosa reticularis | An ectodermal dysplasia characterized by reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy that has_material_basis_in heterozygous mutation in the KRT14 gene on chromosome 17q21.2. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:2121 | ectodermal dysplasia | A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings. |