Hydrocephalus, congenital, 3, with brain anomalies

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Subtype of: Congenital hydrocephalus · Hydrocephalus
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Hydrocephalus, congenital, 3, with brain anomalies
MONDO_0054794
WDR81 Causal
28556411
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Hydrocephalus, congenital, 3, with brain anomalies.
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Congenital communicating hydrocephalus 1 shared geneWDR81 Related via 1 shared gene including WDR81. Microlissencephaly 1 shared geneWDR81 Related via 1 shared gene including WDR81. Cerebellar ataxia, impaired intellectual development, and dysequilibrium 1 shared geneWDR81 Related via 1 shared gene including WDR81. Dysequilibrium syndrome 1 shared geneWDR81 Related via 1 shared gene including WDR81. Omphalocele exstrophy imperforate anus 1 shared geneWDR81 Related via 1 shared gene including WDR81.