li-fraumeni syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal dominant disease characterized by increases risk of developing several types of cancer, including breast cancer, osteosarcomata and soft tissue sarcomata. (Human Disease Ontology, DOID_3012)
External Link http://www.omim.org/entry/151623
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Genes

2 genes associated with the li-fraumeni syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CHEK2 checkpoint kinase 2
TP53 tumor protein p53