Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies

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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 dysmorphic facies and distal skeletal anomalies
EFO_0010659
ZMIZ1 Causal
30639322 31879022
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies.
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Growth abnormality 1 shared geneZMIZ1 Related via 1 shared gene including ZMIZ1. Abnormality of the urinary system 1 shared geneZMIZ1 Related via 1 shared gene including ZMIZ1. Abnormality of head or neck 1 shared geneZMIZ1 Related via 1 shared gene including ZMIZ1. Abnormality of the cardiovascular system 1 shared geneZMIZ1 Related via 1 shared gene including ZMIZ1. Abnormality of the skeletal system 1 shared geneZMIZ1 Related via 1 shared gene including ZMIZ1.