neurodevelopmental disorder with speech delay, movement abnormalities, and seizures

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neurodevelopmental disorder with speech delay, movement abnormalities, and seizures
UNC13A Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with neurodevelopmental disorder with speech delay, movement abnormalities, and seizures.
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neurodevelopmental disorder with hypotonia, epilepsy, and absent speech 1 shared geneUNC13A Related via 1 shared gene including UNC13A. Congenital nervous system disorder 1 shared geneUNC13A Related via 1 shared gene including UNC13A. Developmental regression 1 shared geneUNC13A Related via 1 shared gene including UNC13A. Febrile convulsion 1 shared geneUNC13A Related via 1 shared gene including UNC13A. Benign prostatic hyperplasia 1 shared geneUNC13A Related via 1 shared gene including UNC13A.