Myoclonic dystonia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Myoclonus-dystonia syndrome (MDS) is a rare movement disorder characterized by mild to moderate dystonia along with 'lightning-like' myoclonic jerks. (Orphanet Rare Disease Ontology, Orphanet_36899)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536096
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Genes

2 genes/proteins associated with the disease Myoclonic dystonia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DRD2 dopamine receptor D2 2.88009
SGCE sarcoglycan, epsilon 2.88009