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Cell Culture Ontology
Last uploaded:
July 23, 2014
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| Preferred Name | obsolete_Ehlers-Danlos syndrome, classic type | |
| Synonyms |
EDS, classic type |
|
| Definitions |
Ehlers-Danlos syndrome, classic type (cEDS) is a form of Ehlers-Danlos syndrome (EDS; see this term) that affects the soft connective tissue and is characterized by skin hyperextensibility, widened atrophic scars and joint hypermobility. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_287 |
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| Obsolete |
true |
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| database_cross_reference |
ICD10:Q79.6 OMIM:130000 OMIM:130010
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|
| definition |
Ehlers-Danlos syndrome, classic type (cEDS) is a form of Ehlers-Danlos syndrome (EDS; see this term) that affects the soft connective tissue and is characterized by skin hyperextensibility, widened atrophic scars and joint hypermobility.
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|
| definition_citation |
orphanet
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|
| deprecated |
true
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| has_exact_synonym |
EDS, classic type
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|
| label |
obsolete_Ehlers-Danlos syndrome, classic type
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|
| obsoleted_in_version |
3.41.0
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|
| preferred label |
obsolete_Ehlers-Danlos syndrome, classic type
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|
| prefLabel |
obsolete_Ehlers-Danlos syndrome, classic type
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|
| reason_for_obsolescence |
Replaced with Mondo term.
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| term replaced by | ||
| subClassOf |
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| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |
Create mapping
| Mapping To | Ontology | Source |
|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_287 | HSPO | SAME_URI |
| http://www.orpha.net/ORDO/Orphanet_287 | EFO | SAME_URI |
| http://www.orpha.net/ORDO/Orphanet_287 | ORDO | SAME_URI |
| http://www.orpha.net/ORDO/Orphanet_287 | HOOM | SAME_URI |
| http://www.orpha.net/ORDO/Orphanet_287 | HSPO | LOOM |
| http://www.orpha.net/ORDO/Orphanet_287 | EFO | LOOM |