Hamartoma Syndrome, Multiple Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006223
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Genes

3 genes/proteins associated with the disease Hamartoma Syndrome, Multiple from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FGFR2 fibroblast growth factor receptor 2 2.88009
PTEN phosphatase and tensin homolog 2.88009
BMPR1A bone morphogenetic protein receptor, type IA 2.88009