Crohn's disease phenotype
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (4)
Papers in which this entity is mentioned.
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. (2012)
- Myeloid cells in tumor inflammation. (2012)
- ToppGene Suite for gene list enrichment analysis and candidate gene prioritization. (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 |
|---|---|---|---|
| crohn's disease | phenotype | 34 | 57 |
| crohns disease | phenotype | 2 | 2 |
| crohn disease | phenotype | — | — |
| crohn×s disease | phenotype | — | — |