neurodevelopmental disorder with hypotonia, epilepsy, and absent speech

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
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.
5 View disease cluster →
neurodevelopmental disorder with speech delay, movement abnormalities, and seizures 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.