Syndromic neurodevelopmental disorder with distinctive facial dysmorphism

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Subtype of: Facial dysmorphism syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
syndromic neurodevelopmental disorder with distinctive facial dysmorphism
MONDO_0029143
CCNK Unknown
30122539
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Syndromic neurodevelopmental disorder with distinctive facial dysmorphism.
2 View disease cluster →
Intellectual developmental disorder with hypertelorism and distinctive facies 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.