Propionic Acidemia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An organic acidemia that involes a nonfunctional propionyl CoA carboxylase affecting conversion of aminio acids and fats into sugar for energy. (Human Disease Ontology, DOID_14701)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D056693
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Genes

2 genes/proteins associated with the disease Propionic Acidemia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PCCB propionyl CoA carboxylase, beta polypeptide 2.88009
PCCA propionyl CoA carboxylase, alpha polypeptide 2.88009