PONTOCEREBELLAR HYPOPLASIA, TYPE 4 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description NT MGI. (Human Disease Ontology, DOID_0060273)
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:225753
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease PONTOCEREBELLAR HYPOPLASIA, TYPE 4 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TSEN54 TSEN54 tRNA splicing endonuclease subunit 2.88009