cerebral white matter atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of atrophy (wasting) of the cerebral white matter. (Human Phenotype Ontology, HP_0012762)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012762
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6 genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIMP1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
FAM126A family with sequence similarity 126, member A
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
L2HGDH L-2-hydroxyglutarate dehydrogenase
LMNB1 lamin B1