Neurodevelopmental disorder with hypotonia, seizures, and absent language

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Subtype of: Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with hypotonia, seizures, and absent language
MONDO_0014995
HECW2 Causal
27389779 34321324 27334371 35753050
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with hypotonia, seizures, and absent language.
5 View disease cluster →
Congenital neurologic anomalies 1 shared geneHECW2 Related via 1 shared gene including HECW2. Complex neurodevelopmental disorder 1 shared geneHECW2 Related via 1 shared gene including HECW2. Developmental disability 1 shared geneHECW2 Related via 1 shared gene including HECW2. Non-specific syndromic intellectual disability 1 shared geneHECW2 Related via 1 shared gene including HECW2. Neurodevelopmental disorder 1 shared geneHECW2 Related via 1 shared gene including HECW2.