Hereditary elliptocytosis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
ELLIPTOCYTOSIS 1
611804C2678497MESH:C567520MONDO:0012731
EPB41 Causal — CTD, ClinVar, Disgenet, GenCC, HPO
ELLIPTOCYTOSIS 2
130600C1851741MESH:C565058MONDO:0007533
SPTA1 Causal
1679439 18218854 2328319
CTD, ClinVar, Disgenet, GWAS catalog, HPO
ELLIPTOCYTOSIS 3
617948C1866810MONDO:0054780
SPTB Causal
2070088 32256302 7883966 9005995
CTD, ClinVar, Disgenet, HPO
All7 Causal3 Unknown7
Related Diseases Diseases that share the most curated genes with Hereditary elliptocytosis.
5 View disease cluster →
Spherocytosis 4 shared genesSPTA1, SPTB, SLC4A1, OR10Z1 Related via 4 shared genes including SPTA1, SPTB, SLC4A1. Neonatal anemia 1 shared geneSPTB Related via 1 shared gene including SPTB. Perinatal hemolytic anemia 1 shared geneSPTB Related via 1 shared gene including SPTB. Cerebellar cortical atrophy 1 shared geneMYO5A Related via 1 shared gene including MYO5A. Cryohydrocytosis 1 shared geneSLC4A1 Related via 1 shared gene including SLC4A1.