Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and 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 disorder with regression, abnormal movements, loss of speech, and seizures
MONDO_0060759
IRF2BPL Causal
25363768 28135719 30166628 30057031
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures.
5 View disease cluster →
Regressive neurodevelopmental disorder dystonia seizures 1 shared geneIRF2BPL Related via 1 shared gene including IRF2BPL. Neurodegenerative disease 1 shared geneIRF2BPL Related via 1 shared gene including IRF2BPL. Spastic paraplegia 1 shared geneIRF2BPL Related via 1 shared gene including IRF2BPL. Global developmental delay 1 shared geneIRF2BPL Related via 1 shared gene including IRF2BPL. Atrial fibrillation 1 shared geneIRF2BPL Related via 1 shared gene including IRF2BPL.