Abstract
Traditional classification of genetic diseases as monogenic and polygenic has lagged far behind scientific progress. In this opinion article, we propose and define a new terminology, genetically transitional disease (GTD), referring to cases where a large-effect mutation is necessary, but not sufficient, to cause disease. This leads to a working disease nosology based on gradients of four types of genetic architecture: monogenic, polygenic, GTD, and mixed. We present four scenarios under which GTD may occur; namely, subsets of traditionally Mendelian disease, modifiable Tier 1 monogenic conditions, variable penetrance, and situations where a genetic mutational spectrum produces qualitatively divergent pathologies. The implications of the new nosology in precision medicine are discussed, in which therapeutic options may target the molecular cause or the disease phenotype.
| Original language | English |
|---|---|
| Pages (from-to) | 98-108 |
| Number of pages | 11 |
| Journal | Trends in Genetics |
| Volume | 39 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2023 |
| Externally published | Yes |
Keywords
- expressivity
- genetic disease
- genetically transitional disease
- monogenic
- penetrance
- polygenic risk score
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