|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Atelosteogenesis III (AOIII) is a skeletal dysplasia characterized by short limbs dysmorphic facies and diagnostic radiographic findings. (Orphanet Rare Disease Ontology, Orphanet_56305)|
|Downloads & Tools|
1 genes/proteins associated with the disease ATELOSTEOGENESIS, TYPE III from the curated CTD Gene-Disease Associations dataset.
|FLNB||filamin B, beta||2.88009|