pontocerebellar hypoplasia type 2a Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description NT MGI. (Human Disease Ontology, DOID_0060267)
External Link http://www.omim.org/entry/277470
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Genes

1 genes associated with the pontocerebellar hypoplasia type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TSEN54 TSEN54 tRNA splicing endonuclease subunit