postnatal macrocephaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The postnatal development of an abnormally large skull (macrocephaly). (Human Phenotype Ontology, HP_0005490)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005490
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Genes

2 genes associated with the postnatal macrocephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MED12 mediator complex subunit 12
PTEN phosphatase and tensin homolog