Obstructive Hydrocephalus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0549423
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Genes

16 genes associated with the disease Obstructive Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AQP1 aquaporin 1 (Colton blood group)
AQP4 aquaporin 4
CCDC88C coiled-coil domain containing 88C
CCND2 cyclin D2
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
EPO erythropoietin
HYDIN HYDIN, axonemal central pair apparatus protein
IFT122 intraflagellar transport 122
ISPD isoprenoid synthase domain containing
LAMC2 laminin, gamma 2
MAGEL2 melanoma antigen family L2
MYO9A myosin IXA
PRL prolactin
RND3 Rho family GTPase 3
SIN3A SIN3 transcription regulator family member A
UBE2D1 ubiquitin-conjugating enzyme E2D 1