Pontocerebellar Hypoplasia Type 3 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description NT MGI. (Human Disease Ontology, DOID_0060272)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C548072
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Genes

1 genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 3 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CLAM cerebellar atrophy with progressive microcephaly 2.88009