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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