| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A collagen disease and a monogenic 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. (Human Disease Ontology, DOID_13359) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D004535 |
| Similar Terms | |
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2 genes/proteins associated with the disease Ehlers-Danlos Syndrome from the curated CTD Gene-Disease Associations dataset.
