fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies
ATP1A2 Causal
31608932 30690204
ClinGen
All1 Causal1 Unknown0
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hemiplegic migraine-developmental and epileptic encephalopathy spectrum 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2. Alternating hemiplegia of childhood 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2. Benign neonatal epilepsy 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2. Dysphasia 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2. Hemiplegic migraine 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2.