Neurodevelopmental disorder with severe motor impairment and absent language

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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 severe motor impairment and absent language
MONDO_0060622MONDO_0859266
DHX30 Causal
28327206 29100085 34020708 34145223 34180050 36643085 37094863 38366977
ClinGen, Open Targets —
  • neurodevelopmental disorder with severe motor impairment and absent language
MONDO_0060622MONDO_0859266
TAF8 Unknown
29648665 35759269 39169228
Open Targets
All2 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with severe motor impairment and absent language.
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Partial agenesis of corpus callosum 1 shared geneTAF8 Related via 1 shared gene including TAF8. Hyperpituitarism 1 shared geneTAF8 Related via 1 shared gene including TAF8. Strabismus 1 shared geneDHX30 Related via 1 shared gene including DHX30. Seborrheic dermatitis 1 shared geneTAF8 Related via 1 shared gene including TAF8. Amyotrophic lateral sclerosis 1 shared geneTAF8 Related via 1 shared gene including TAF8.