Intellectual developmental disorder with language impairment and with or without autistic features

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Subtype of: Intellectual developmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
intellectual developmental disorder with language impairment and autistic features
MONDO_0013352
FOXP1 Causal
20950788 22670142 24214399 25853299 28735298 28884888 29090079 29330474 30092897
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Intellectual developmental disorder with language impairment and with or without autistic features.
5 View disease cluster →
Congenital aortic valve atresia 1 shared geneFOXP1 Related via 1 shared gene including FOXP1. Congenital mitral valve atresia 1 shared geneFOXP1 Related via 1 shared gene including FOXP1. Intellectual developmental disorder language autism 1 shared geneFOXP1 Related via 1 shared gene including FOXP1. Mental retardation with language impairment and autistic features 1 shared geneFOXP1 Related via 1 shared gene including FOXP1. Intellectual developmental disorder seizures hypotonia skeletal 1 shared geneFOXP1 Related via 1 shared gene including FOXP1.