loading...| Preferred Name | Hyperostosis, Cortical, Congenital [Disease/Finding] | |
| Synonyms |
Hyperostosis, Cortical, Congenital Familial Infantile Cortical Hyperostosis Cortical Congenital Hyperostosis Infantile Cortical Hyperostosis Familial Caffey's Disease Caffey Disease Congenital Hyperostosis, Cortical Cortical Hyperostosis, Congenital Caffey-De Toni-Silvermann Syndrome |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001601 |
|
| altLabel |
Hyperostosis, Cortical, Congenital Familial Infantile Cortical Hyperostosis Cortical Congenital Hyperostosis Infantile Cortical Hyperostosis Familial Caffey's Disease Caffey Disease Congenital Hyperostosis, Cortical Cortical Hyperostosis, Congenital Caffey-De Toni-Silvermann Syndrome |
|
| cui |
C0020497 |
|
| MESH DEFINITION |
A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed) |
|
| MESH DUI |
D006958 |
|
| MeSH name |
Hyperostosis, Cortical, Congenital |
|
| MESH UI |
M0010841 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000001601 |
|
| NUI |
N0000001601 |
|
| prefLabel |
Hyperostosis, Cortical, Congenital [Disease/Finding] |
|
| SNOMED CID |
24752008 |
|
| tui |
T047 |
|
| subClassOf |