increased hamartoma incidence Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the expected number of benign focal malformations in a specific population in a given time period; results from faulty development of an organ, and is composed of an abnormal mixture of tissue elements, or an abnormal proportion of a single element normally present at that site (Mammalian Phenotype Ontology, MP_0010306)
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5 gene mutations causing the increased hamartoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDX2 caudal type homeobox 2
PKD1 polycystic kidney disease 1 (autosomal dominant)
PTEN phosphatase and tensin homolog
STK11 serine/threonine kinase 11
TP53 tumor protein p53