CDH10 gene
Evidence from:
primary |
all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| CDH10 | associated_with | anorexia nervosa | — | 1 |
| CDH10 | associated_with | ASD | — | 1 |
| CDH10 | associated_with | autism | — | 1 |
| CDH10 | risk_factor_for | autism spectrum disorder | — | 1 |
| CDH10 | associated_with | OCD | — | 1 |
Mentioned in (4)
Papers in which this entity is mentioned.
- DNA methylation signature of human fetal alcohol spectrum disorder. (2016)
- Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. (2015)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. (2009)
Merged raw entities (2)
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 |
|---|---|---|---|
| cdh10 | gene | 4 | 10 |
| cadherin 10 | gene | — | — |