loading...| Preferred Name |
obsolete_Werner syndrome |
|
| Synonyms |
WS Adult progeria |
|
| Definitions |
Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_902 |
|
| Obsolete |
true |
|
| database_cross_reference |
MeSH:D014898 MedDRA:10049429 UMLS:C0043119 OMIM:277700 ICD10:E34.8 |
|
| definition |
Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders. |
|
| definition_citation |
orphanet |
|
| deprecated |
true |
|
| has_exact_synonym |
Adult progeria WS |
|
| label |
obsolete_Werner syndrome |
|
| obsoleted_in_version |
3.41.0 |
|
| prefLabel |
obsolete_Werner syndrome |
|
| reason_for_obsolescence |
Replaced with Mondo term. |
|
| term replaced by | ||
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_902 | ORDO | SAME_URI |