Disease #05212 (AMDME (ataxia, myoclonia, dysarthria, muscle weakness, exercise intolerance))
| Official abbreviation |
AMDME |
| Name |
ataxia, myoclonia, dysarthria, muscle weakness, exercise intolerance |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
SLC25A32 |
| Associated tissues |
brain;skeletal muscle |
| Disease features |
severe neuromuscular phenotype |
| Remarks |
- |
| Date created |
2016-12-22 09:52:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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