Skraban-deardorff syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SKRABAN-DEARDORFF SYNDROME
617616C4539927MONDO:0054636
WDR26 Causal
28686853 36076104 38710080
ClinGen, ClinVar, Disgenet, GWAS catalog, HPO —
WDR62 Causal — Disgenet —
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Skraban-deardorff syndrome.
5 View disease cluster →
microcephaly 2, primary, autosomal recessive, with or without cortical malformations 1 shared geneWDR62 Related via 1 shared gene including WDR62. Intellectual developmental disorder seizures dysmorphic gait 1 shared geneWDR26 Related via 1 shared gene including WDR26. Polymicrogyria 1 shared geneWDR62 Related via 1 shared gene including WDR62. Cortical development malformation 1 shared geneWDR62 Related via 1 shared gene including WDR62. Congenital microcephaly 1 shared geneWDR62 Related via 1 shared gene including WDR62.