|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormal reduction of the cell motility of neutrophils. (Human Phenotype Ontology, HP_0005400)|
|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.
|SLC35C1||solute carrier family 35 (GDP-fucose transporter), member C1|