meniere disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A vestibular disease characterized by vertigo, low-pitched tinnitus and hearing loss. (Human Disease Ontology, DOID_9849)
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Genes

10 genes associated with the disease meniere disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AQP1 aquaporin 1 (Colton blood group)
AQP2 aquaporin 2 (collecting duct)
AQP3 aquaporin 3 (Gill blood group)
AQP4 aquaporin 4
CTLA4 cytotoxic T-lymphocyte-associated protein 4
HCFC1 host cell factor C1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HSPA1A heat shock 70kDa protein 1A
PARP1 poly (ADP-ribose) polymerase 1
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)