pontocerebellar hypoplasia, type 6 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description NT MGI. (Human Disease Ontology, DOID_0060275)
External Link http://www.omim.org/entry/611523
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Genes

1 genes associated with the pontocerebellar hypoplasia, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
RARS2 arginyl-tRNA synthetase 2, mitochondrial