complex disorders phenotype
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| candidate genes | risk_factor_for | complex disorders | — | 1 |
Mentioned in (5)
Papers in which this entity is mentioned.
- CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (2024)
- Polygenic risk scores: from research tools to clinical instruments. (2020)
- Gene-environment interactions in development and disease. (2017)
- Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence. (2014)
- Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
Merged raw entities (4)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| complex disorders | phenotype | 9 | 15 |
| complex disorder | phenotype | 4 | 4 |
| multifactorial disorders | phenotype | — | — |
| multigenic disorders | phenotype | — | — |