Disease #00156 (EPM11 (Progressive Myoclonic Epilepsy 11), OMIM:618876)
Official abbreviation |
EPM11 |
Name |
Progressive Myoclonic Epilepsy 11 |
OMIM ID |
618876 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SEMA6B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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