diffuse white matter abnormalities Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description This finding is demonstrated by cerebral computer tomography or magnetic resonance imaging. (Human Phenotype Ontology, HP_0007204)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007204
Similar Terms
Downloads & Tools

Genes

1 genes associated with the diffuse white matter abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HTRA1 HtrA serine peptidase 1