affected status phenotype
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (3)
Papers in which this entity is mentioned.
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. (2013)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
Merged raw entities (1)
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 |
|---|---|---|---|
| affected status | phenotype | 3 | 3 |