Reticulocytosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An elevation in the number of reticulocytes (immature erythrocytes) in the peripheral blood circulation. (Human Phenotype Ontology, HP_0001923)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D045262
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Genes

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

Symbol Name Standardized Value
SOD2 superoxide dismutase 2, mitochondrial 2.88009
PARK7 parkinson protein 7 2.88009