Autonomic Bladder Dysfunction Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormal bladder function (increased urge or frequency of urination or urge incontinence) resulting from abnormal functioning of the autonomic nervous system. (Human Phenotype Ontology, HP_0005341)
External Link https://www.disgenet.org/browser/0/1/0/C4025212
Similar Terms
Downloads & Tools

Genes

5 genes associated with the disease Autonomic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
B2M beta-2-microglobulin
COQ2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
LMNB1 lamin B1
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
USP7 ubiquitin specific peptidase 7 (herpes virus-associated)