Intellectual developmental disorder with hypertelorism and distinctive facies

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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 hypertelorism and distinctive facies
MONDO_0029143
CCNK Causal
41101726 37597256 35063350 30122539
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Intellectual developmental disorder with hypertelorism and distinctive facies.
2 View disease cluster →
Syndromic neurodevelopmental disorder with distinctive facial dysmorphism 1 shared geneCCNK Related via 1 shared gene including CCNK. Intellectual developmental disorder dysmorphic facial 1 shared geneCCNK Related via 1 shared gene including CCNK.