Cushing's symphalangism Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal dominant disease that is characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive deafness. (Human Disease Ontology, DOID_0050788)
External Link http://www.omim.org/entry/185800
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Genes

1 genes associated with the Cushing's symphalangism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
NOG noggin