diffuse cerebral atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Diffuse unlocalised atrophy affecting the cerebrum. (Human Phenotype Ontology, HP_0002506)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002506
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Genes

7 genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BTD biotinidase
CTSF cathepsin F
FMR1 fragile X mental retardation 1
GALC galactosylceramidase
GLB1 galactosidase, beta 1
MED17 mediator complex subunit 17
TBP TATA box binding protein