| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A leukodystrophy that is characterized by the destruction of white matter and the formation of Rosenthal fibers consisting of abnormal clumps of protein that accumulate in astrocytes. (Human Disease Ontology, DOID_4252) |
| External Link | http://www.omim.org/entry/203450 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the alexander disease phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| GFAP | glial fibrillary acidic protein |
