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loading...| Preferred Name |
Arthrogryposis [Disease/Finding] |
|
| Synonyms |
Otto Syndrome |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000000483 |
|
| altLabel |
Otto Syndrome Congenital Multiple Arthrogryposis Congenital Arthromyodysplasia Guérin-Stern Syndrome Amyoplasia Congenita Rocher-Sheldon Syndrome Fibrous Ankylosis of Multiple Joints Rossi Syndrome Arthromyodysplasia, Congenital Arthrogryposis Multiplex Congenita Arthrogryposis Guerin-Stern Syndrome Arthrogryposis Multiplex Congenita (AMC) Myodystrophia Fetalis Deformans |
|
| cui |
C0003886 |
|
| MESH DEFINITION |
Persistent flexure or contracture of a joint. |
|
| MESH DUI |
D001176 |
|
| MeSH name |
Arthrogryposis |
|
| MESH UI |
M0001754 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000000483 |
|
| NUI |
N0000000483 |
|
| prefLabel |
Arthrogryposis [Disease/Finding] |
|
| SNOMED CID |
111246005 205403009 |
|
| tui |
T047 |
|
| subClassOf |
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