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