|Dataset||GWASdb SNP-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||Absence or underdevelopment of tissue in the central nervous system. (Human Phenotype Ontology, HP_0002977)|
|Downloads & Tools|
2 genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.