| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | One of the three types of glia cells that, with the nerve cells, compose the central nervous system and are characterized by sheetlike processes that wrap around individual axons to form the myelin sheath of nerve fibers. (Human Phenotype Ontology, HP_0100706) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0100706 |
| Similar Terms | |
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1 genes associated with the abnormality of the oligodendroglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PLP1 | proteolipid protein 1 |
