Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures

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Subtype of: Neurodevelopmental disorder · Seizures
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures
MONDO_0859282
CHKA Causal
35202461
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures.
5 View disease cluster →
Abnormal muscle tone 1 shared geneCHKA Related via 1 shared gene including CHKA. Abnormality of movement 1 shared geneCHKA Related via 1 shared gene including CHKA. Short stature 1 shared geneCHKA Related via 1 shared gene including CHKA. Nonsyndromic intellectual disability 1 shared geneCHKA Related via 1 shared gene including CHKA. Microcephaly 1 shared geneCHKA Related via 1 shared gene including CHKA.