Jump to:
loading...| Preferred Name |
Werner Syndrome [Disease/Finding] |
|
| Synonyms |
Werners Syndrome |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003159 |
|
| altLabel |
Werners Syndrome Adult Premature Aging Syndrome Werner's Syndrome Progeria, Adult Werner Syndrome Adult Progeria |
|
| cui |
C0043119 |
|
| MESH DEFINITION |
An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, baldness, and a high incidence of neoplastic disease. |
|
| MESH DUI |
D014898 |
|
| MeSH name |
Werner Syndrome |
|
| MESH UI |
M0022920 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000003159 |
|
| NUI |
N0000003159 |
|
| prefLabel |
Werner Syndrome [Disease/Finding] |
|
| SNOMED CID |
51626007 |
|
| tui |
T047 |
|
| subClassOf |
Create mapping