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Ovalocytosis, southeast asian
Ovalocytosis, southeast asian
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Ovalocystois, SA type
MONDO_0008165
SLC4A1
Unknown
9600966
9312167
Open Targets
Collecting duct acid secretion
Erythrocytes take up carbon dioxide and release oxygen
Erythrocytes take up oxygen and release carbon dioxide
Bicarbonate transporters
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA)
+2 more
Ovalocytosis, Southeast Asian
MONDO_0008165
SLC4A1
Unknown
1538405
1722314
36320073
Open Targets
Collecting duct acid secretion
Erythrocytes take up carbon dioxide and release oxygen
Erythrocytes take up oxygen and release carbon dioxide
Bicarbonate transporters
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA)
+2 more
All
1
Causal
0
Unknown
1
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Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
Related Diseases
Diseases that share the most curated genes with Ovalocytosis, southeast asian.
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View disease cluster →
Ovalocytosis, sa type cryohydrocytosis
1 shared gene
SLC4A1
Related via 1 shared gene including SLC4A1.
Spherocytoisis type 4
1 shared gene
SLC4A1
Related via 1 shared gene including SLC4A1.
Cryohydrocytosis
1 shared gene
SLC4A1
Related via 1 shared gene including SLC4A1.
Hereditary xerocytosis
1 shared gene
SLC4A1
Related via 1 shared gene including SLC4A1.
Xerocytosis
1 shared gene
SLC4A1
Related via 1 shared gene including SLC4A1.
1
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