15q13.3 deletion variant
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 15q13.3 deletion | associated_with | autism | — | 1 |
| 15q13.3 deletion | associated_with | mental retardation | — | 1 |
| 15q13.3 deletion | risk_factor_for | schizophrenia | — | 1 |
| 15q13.3 deletion | associated_with | schizophrenia | — | 1 |
Mentioned in (3)
Papers in which this entity is mentioned.
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
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 |
|---|---|---|---|
| 15q13.3 deletion | variant | 3 | 3 |
| 15q13.3 microdeletion | variant | — | — |
| deletion at 15q13.3 | variant | — | — |
| deletions at chr15q13.3 | variant | — | — |