Curry-Hall syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Acrofacial dysostosis, Weyers type (WAD) is a rare ectodermal dysplasia syndrome with bone abnormalities, characterized by postaxial polydactyly, onychodystrophy, dental anomalies, and a mild short stature associated with normal intelligence. (Orphanet Rare Disease Ontology, Orphanet_952)
External Link http://www.omim.org/entry/193530
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Genes

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

Symbol Name
EVC2 Ellis van Creveld syndrome 2