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

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Subtype of: Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities
  • Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities
MONDO_0030837
NARS1 Causal
32738225 32788587
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities.
3 View disease cluster →
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.