loading...| Preferred Name | Ehlers-Danlos syndrome | |
| Synonyms |
elastic skin Cutis hyperelastica |
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| Definitions |
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. OMIM mapping confirmed by DO. [LS]. OMIM mapping by NeuroDevNet. [LS]. |
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| ID |
http://purl.obolibrary.org/obo/DOID_13359 |
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| comment |
OMIM mapping confirmed by DO. [LS]. OMIM mapping by NeuroDevNet. [LS]. |
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| database_cross_reference |
ICD9CM:756.83 ICD10CM:Q79.6 MIM:PS130000 SNOMEDCT_US_2023_03_01:268352002 MESH:D004535 UMLS_CUI:C0013720 GARD:6322 NCI:C34568 |
|
| definition |
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. |
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| has exact synonym |
elastic skin Cutis hyperelastica |
|
| has_alternative_id |
DOID:14696 |
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| has_obo_namespace |
disease_ontology |
|
| id |
DOID:13359 |
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| in_subset | ||
| label |
Ehlers-Danlos syndrome |
|
| notation |
DOID:13359 |
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| prefLabel |
Ehlers-Danlos syndrome |
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| subClassOf |