Hemoglobin h disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
HEMOGLOBIN H DISEASE
61397893616C3161174MONDO:0013512
HBA1 Causal — ClinVar, Disgenet, GenCC, HPO, Orphanet
HBA2 Causal — ClinVar, Disgenet, GenCC, HPO, Orphanet
HEMOGLOBIN H DISEASE, NONDELETIONAL
C3279561
HBA1 Causal
10569720
Disgenet
HBA2 Causal
10569720
Disgenet
All3 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Hemoglobin h disease.
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Alpha thalassemia 3 shared genesHBA1, HBA2, ATRX Related via 3 shared genes including HBA1, HBA2, ATRX. Hemoglobin barts fetalis syndrome 3 shared genesHBA1, HBA2, ATRX Related via 3 shared genes including HBA1, HBA2, ATRX. methemoglobinemia, alpha type 2 shared genesHBA1, HBA2 Related via 2 shared genes including HBA1, HBA2. erythrocytosis, familial, 7 2 shared genesHBA1, HBA2 Related via 2 shared genes including HBA1, HBA2. Hemoglobin m disease 2 shared genesHBA1, HBA2 Related via 2 shared genes including HBA1, HBA2.