Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=C3151610
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
ROR2 receptor tyrosine kinase-like orphan receptor 2