Parietal Foramina Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description NT MGI. (Human Disease Ontology, DOID_0060285)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C566826
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Genes

2 genes/proteins associated with the disease Parietal Foramina from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MSX2 msh homeobox 2 2.88009
ALX4 ALX homeobox 4 2.88009