Disease #05849 (DYT28 (dystonia, type 28, childhood-onset (DYT28)), OMIM:617284)
| Official abbreviation |
DYT28 |
| Name |
dystonia, type 28, childhood-onset (DYT28) |
| OMIM ID |
617284 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
KMT2B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-09-30 10:31:09 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
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