PTCHD1 gene
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| PTCHD1 | associated_with | autism spectrum disorder | — | 1 |
Mentioned in (4)
Papers in which this entity is mentioned.
- Identification of novel candidate disease genes from de novo exonic copy number variants. (2017)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- Facial phenotypes in subgroups of prepubertal boys with autism spectrum disorders are correlated with clinical phenotypes. (2011)
- Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (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 |
|---|---|---|---|
| ptchd1 | gene | 4 | 11 |
| patched domain containing 1 | gene | — | — |