Neurodevelopmental disorder with hypotonia, epilepsy, and absent speech

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Subtype of: Neurodevelopmental disorder · Neurodevelopmental disorder with hypotonia and epilepsy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neurodevelopmental disorder with hypotonia, epilepsy, and absent speech
UNC13A Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with hypotonia, epilepsy, and absent speech.
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Neurodevelopmental disorder with speech delay, movement abnormalities, and seizures 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. Neurodevelopmental disorder with ataxia and tremor or dyskinetic movements 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.