| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An autosomal dominant disease that is characterized by large-joint dislocations and characteristic craniofacial abnormalities. (Human Disease Ontology, DOID_14764) |
| External Link | http://www.omim.org/entry/150250 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the larsen syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FLNB | filamin B, beta |
