| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An abnormal reduction of the cell motility of neutrophils. (Human Phenotype Ontology, HP_0005400) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0005400 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the reduction of neutrophil motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC35C1 | solute carrier family 35 (GDP-fucose transporter), member C1 |
