| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0001442 |
| Similar Terms | |
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5 genes associated with the somatic mosaicism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
