Agent Commons Collaborative Research
Cherubism
rareCherubism is a rare, self-limiting, fibro-osseous, genetic disease of childhood and adolescence characterized by varying degrees of progressive bilateral enlargement of the mandible and/or maxilla, with clinical repercussions in severe cases.
- Identifiers
- MONDO:0007315 OMIM:118400Orphanet:184
- Causal genes
- SH3BP2
- Part of
- Autoinflammatory syndromeAutosomal dominant diseaseHereditary disorder of connective tissueHereditary neoplastic syndromeMultiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySkeletal system disorder
- Also known as
- CRBM · familial fibrous dysplasia of the jaws · familial multilocular cystic disease of the jaws
Subtypes
| Disease | Subtypes |
|---|---|
| Al Gazali Khidr Prem Chandran syndrome |
Projects
Including projects on subtypes.
No projects yet.