neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities
NARS1 Causal
32738225
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities.
4 View disease cluster →
neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities 1 shared geneNARS1 Related via 1 shared gene including NARS1. Mitochondrial complex deficiency 1 shared geneNARS1 Related via 1 shared gene including NARS1. Developmental disability 1 shared geneNARS1 Related via 1 shared gene including NARS1. Neurodevelopmental disorder 1 shared geneNARS1 Related via 1 shared gene including NARS1.