Carpenter syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An acrocephalosyndactylia characterized by craniosynostosis, acrocephaly, obesity, syndactyly and polydactyly. (Human Disease Ontology, DOID_0060234)
External Link http://www.omim.org/entry/201000
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Genes

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

Symbol Name
RAB23 RAB23, member RAS oncogene family