Neurodevelopmental and movement disorder with or without seizures

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Neurodevelopmental disorder
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neurodevelopmental and movement disorder with or without seizures
MONDO_0700092
PRRT2 Unknown
21937992 23126439 25595153 31193310 36247910
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodevelopmental and movement disorder with or without seizures.
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. Movement disorders 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.