Neurodevelopmental disorder with ataxia and tremor or dyskinetic movements

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 disorder with ataxia and tremor or dyskinetic movements
MONDO_0100038
UNC13A Unknown
28192369 41125872
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with ataxia and tremor or dyskinetic movements.
5 View disease cluster →
Neurodevelopmental disorder with speech delay, movement abnormalities, and seizures 1 shared geneUNC13A Related via 1 shared gene including UNC13A. Neurodevelopmental disorder with hypotonia, epilepsy, and absent speech 1 shared geneUNC13A Related via 1 shared gene including UNC13A. Congenital epileptic encephalopathy and severe neuromuscular disorder 1 shared geneUNC13A Related via 1 shared gene including UNC13A. Congenital nervous system disorder 1 shared geneUNC13A Related via 1 shared gene including UNC13A. Febrile convulsion 1 shared geneUNC13A Related via 1 shared gene including UNC13A.