pontocerebellar hypoplasia, type 8 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description NT MGI. (Human Disease Ontology, DOID_0060277)
External Link http://www.omim.org/entry/614961
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1 genes associated with the pontocerebellar hypoplasia, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CHMP1A charged multivesicular body protein 1A