Histidinemia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A histidine metabolism disease that involves a deficiency of the enzyme histidase. (Human Disease Ontology, DOID_0060168)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538320
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Histidinemia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HAL histidine ammonia-lyase 2.88009