Disease #00001 (ALXDRD (Alexander Disease), OMIM:203450)
| Official abbreviation |
ALXDRD |
| Name |
Alexander Disease |
| OMIM ID |
203450 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
142 |
| Phenotype entries for this disease |
41 |
| Associated with 1 gene |
GFAP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|
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