Dysgenesis Of The Cerebellar Vermis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Defective development of the vermis of cerebellum. (Human Phenotype Ontology, HP_0002195)
External Link https://www.disgenet.org/browser/0/1/0/C4025719
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Genes

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

Symbol Name
CSPP1 centrosome and spindle pole associated protein 1
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
KIAA0586 KIAA0586
TMEM216 transmembrane protein 216