7 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:17 | musculoskeletal system disease | A disease of anatomical entity that occurs in the muscular and/or skeletal system. |
| DOID:65 | connective tissue disease | A musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage. |
| DOID:13359 | Ehlers-Danlos syndrome | A collagen disease that is characterized by extremely flexible joints, elastic skin, and excessive bruising caused by a heritable defect in collagen synthesis, which leads to marked healing difficulties. EDS has five cardinal signs, which may be present to some degree in all of the subtypes. These five cardinal signs are skin fragility, blood vessel fragility, skin hyperelasticity, joint hypermobility, and characteristic subcutaneous nodules. |
| DOID:854 | collagen disease | A connective tissue disease that characterized by connective tissue disease that has_material_basis_in inheritable defects in collagen. |
| DOID:14757 | Ehlers-Danlos syndrome hypermobility type | An Ehlers-Danlos syndrome that is characterized by joint hyperextensibility without skeletal deformity. |
6 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:13359 | DOID:14757 |
| is_a | DOID:65 | DOID:14757 |
| is_a | DOID:854 | DOID:14757 |
| is_a | DOID:17 | DOID:14757 |
| is_a | DOID:7 | DOID:14757 |
| is_a | DOID:4 | DOID:14757 |
