| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A severe loss of myelin from nerve fibers in the central nervous system. (Human Phenotype Ontology, HP_0007258) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0007258 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the severe demyelination of the white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| L2HGDH | L-2-hydroxyglutarate dehydrogenase |
