Disease #03726 (ETM4 (tremor, hereditary essential, type 4 (ETM4)), OMIM:614782)
| Official abbreviation |
ETM4 |
| Name |
tremor, hereditary essential, type 4 (ETM4) |
| OMIM ID |
614782 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FUS |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-05-15 10:30:00 +02:00 (CEST) |
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