1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0080728 | Ehlers-Danlos syndrome arthrochalasia type 2 | An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the COL1A2 gene on chromosome 7q21. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |