Craniofacial anomalies, corpus callosum dysgenesis, ptosis, and developmental delay

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Subtype of: Dysgenesis of corpus callosum
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
craniofacial anomalies, corpus callosum dysgenesis, ptosis, and developmental delay
MONDO_0032836
ZNF462 Unknown
28513610
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Craniofacial anomalies, corpus callosum dysgenesis, ptosis, and developmental delay.
5 View disease cluster →
Weiss-kruszka syndrome 1 shared geneZNF462 Related via 1 shared gene including ZNF462. Prominent metopic ridge 1 shared geneZNF462 Related via 1 shared gene including ZNF462. Ptosis 1 shared geneZNF462 Related via 1 shared gene including ZNF462. Autistic behavior 1 shared geneZNF462 Related via 1 shared gene including ZNF462. Craniosynostosis 1 shared geneZNF462 Related via 1 shared gene including ZNF462.