Movement disorders

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Subtype of: Movement disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
movement disorders
MONDO_0005395
PRRT2 Unknown
23126439 23352743 21937992 25595153 23398397 36180924
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Movement disorders.
5 View disease cluster →
Familial infantile convulsions with paroxysmal choreoathetosis 1 shared genePRRT2 Related via 1 shared gene including PRRT2. Paroxysmal dystonia 1 shared genePRRT2 Related via 1 shared gene including PRRT2. Infantile convulsions and choreoathetosis 1 shared genePRRT2 Related via 1 shared gene including PRRT2. Neurodevelopmental and movement disorder with or without seizures 1 shared genePRRT2 Related via 1 shared gene including PRRT2. Seizures, benign familial infantile, 2 1 shared genePRRT2 Related via 1 shared gene including PRRT2.