Disease #00007 (DMD (Dystonia Musculorum Deformans), OMIM:128100)
| Official abbreviation |
DMD |
| Name |
Dystonia Musculorum Deformans |
| OMIM ID |
128100 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
173 |
| Phenotype entries for this disease |
- |
| Associated with 11 genes |
ADCY5, ATM, ATP1A3, GCH1, GNAL, PNKD, PRKRA, SGCE, SLC2A1, THAP1, TOR1A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
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