| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Atelosteogenesis III (AOIII) is a skeletal dysplasia characterized by short limbs dysmorphic facies and diagnostic radiographic findings. (Orphanet Rare Disease Ontology, Orphanet_56305) |
| External Link | http://www.omim.org/entry/108721 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the atelosteogenesis, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FLNB | filamin B, beta |
