Abnormality Of The Cerebellar Vermis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An anomaly of the vermis of cerebellum. (Human Phenotype Ontology, HP_0002334)
External Link https://www.disgenet.org/browser/0/1/0/C4025712
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Genes

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

Symbol Name
INPP5K inositol polyphosphate-5-phosphatase K
MYO5A myosin VA (heavy chain 12, myoxin)
PIEZO2 piezo-type mechanosensitive ion channel component 2
SIL1 SIL1 nucleotide exchange factor
SRD5A3 steroid 5 alpha-reductase 3
TRAPPC9 trafficking protein particle complex 9