aplasia/hypoplasia involving the central nervous system Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of tissue in the central nervous system. (Human Phenotype Ontology, HP_0002977)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002977
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Genes

2 genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
WDR41 WD repeat domain 41 1.12851
GMDS GDP-mannose 4,6-dehydratase 0.899912