1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0070522 | peeling skin syndrome 3 | A peeling skin syndrome that has_material_basis_in autosomal recessive inheritance of variation in the chromosome region 19q13. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |