|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||A syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities. (Human Disease Ontology, DOID_0060254)|
|Downloads & Tools|
1 genes associated with the Robinow syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|WNT5A||wingless-type MMTV integration site family, member 5A|