|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The presence of genetically distinct populations of somatic cells in a given organism caused by DNA mutations, epigenetic alterations of DNA, chromosomal abnormalities or the spontaneous reversion of inherited mutations. (Human Phenotype Ontology, HP_0001442)|
|Downloads & Tools|
5 genes associated with the somatic mosaicism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.