pontocerebellar hypoplasia, type 10 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description NT MGI. (Human Disease Ontology, DOID_0060279)
External Link http://www.omim.org/entry/615803
Similar Terms
Downloads & Tools


1 genes associated with the pontocerebellar hypoplasia, type 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CLP1 cleavage and polyadenylation factor I subunit 1