Hamartoma Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A disordered proliferation of mature tissues that is native to the site of origin - eg, exostoses, nevi and soft tissue hamartomas. Although most hamartomas are benign, some histologic subtypes - eg, neuromuscular hamartoma, may proliferate aggressively such as mesenchymal cystic hamartoma, Sclerosing epithelial hamartoma, Sclerosing metanephric hamartoma. (Human Phenotype Ontology, HP_0010566)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006222
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Genes

2 genes/proteins associated with the disease Hamartoma from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1 2.88009
FLCN folliculin 2.88009