Abnormality Of The Mastoid Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the mastoid process, which is the conical prominence projecting from the undersurface of the mastoid portion of the temporal bone. (Human Phenotype Ontology, HP_0000264)
External Link https://www.disgenet.org/browser/0/1/0/C4025872
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Genes

1 genes associated with the disease Abnormality Of The Mastoid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
DLX3 distal-less homeobox 3