pontocerebellar hypoplasia type 1a Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description NT MGI. (Human Disease Ontology, DOID_0060265)
External Link http://www.omim.org/entry/607596
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1 genes associated with the pontocerebellar hypoplasia type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
VRK1 vaccinia related kinase 1