Anemia, congenital, non-spherocytic hemolytic, 1

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Subtype of: Anemia · Congenital nonspherocytic hemolytic anemia · Hemolytic anemia
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Anemia, congenital, non-spherocytic hemolytic, 1
MONDO_0010480
G6PD Unknown
1303180 1303182 1536798 1611091 1889820 1945893 2836867 2912069 7858267 7959695 8193373 8490627 8533762 8733135 9452072 12524354 20007901 26479991 30988594 38066190
Open Targets
All1 Causal0 Unknown1
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G6PD deficiency 1 shared geneG6PD Related via 1 shared gene including G6PD. Anemia, nonspherocytic hemolytic 1 shared geneG6PD Related via 1 shared gene including G6PD. Hemolytic anemia, g6pd deficient (favism) 1 shared geneG6PD Related via 1 shared gene including G6PD. Infections 1 shared geneG6PD Related via 1 shared gene including G6PD. Anhidrotic ectodermal dysplasia with immunodeficiency, osteopetrosis, and lymphedema 1 shared geneG6PD Related via 1 shared gene including G6PD.