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

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/604317
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Genes

1 genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
WDR62 WD repeat domain 62