Robinow syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/180700
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Genes

1 genes associated with the Robinow syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
WNT5A wingless-type MMTV integration site family, member 5A