pontocerebellar hypoplasia, type 2e Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description NT MGI. (Human Disease Ontology, DOID_0060271)
External Link http://www.omim.org/entry/615851
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1 genes associated with the pontocerebellar hypoplasia, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
VPS53 vacuolar protein sorting 53 homolog (S. cerevisiae)