Neurodevelopmental disorder with progressive movement abnormalities

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Subtype of: Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with progressive movement abnormalities
MONDO_0968976
LHX4-AS1 Unknown
32108178 21937992 36457943 37951597 34296759
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with progressive movement abnormalities.
2 View disease cluster →
Autosomal recessive mental retardation 1 shared geneLHX4-AS1 Related via 1 shared gene including LHX4-AS1. Intellectual developmental disorder 1 shared geneLHX4-AS1 Related via 1 shared gene including LHX4-AS1.