microcephaly 2, primary, autosomal recessive, with or without cortical malformations

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Microcephaly 2, primary, autosomal recessive, with or without cortical malformations
WDR62 Causal
20729831 20890278 20890279 21496009
ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with microcephaly 2, primary, autosomal recessive, with or without cortical malformations.
5 View disease cluster →
Skraban-deardorff syndrome 1 shared geneWDR62 Related via 1 shared gene including WDR62. 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. Primary microcephaly 1 shared geneWDR62 Related via 1 shared gene including WDR62.