dysgenesis of the cerebellar vermis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Defective development of the vermis of cerebellum. (Human Phenotype Ontology, HP_0002195)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002195
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Genes

2 genes associated with the dysgenesis of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
TMEM216 transmembrane protein 216