Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C3809394
Disease: DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3 		1 0 1 8.3E-02 0 0
CUI: C3889873
Disease: HEMOGLOBIN SAINT ETIENNE PHENOTYPE
HEMOGLOBIN SAINT ETIENNE PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C3889898
Disease: HEMOGLOBIN C PHENOTYPE
HEMOGLOBIN C PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C3891694
Disease: HEMOGLOBIN TUBINGEN PHENOTYPE
HEMOGLOBIN TUBINGEN PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C4016175
Disease: HEMOGLOBIN HOUSTON PHENOTYPE
HEMOGLOBIN HOUSTON PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C4017494
Disease: BETA-KNOSSOS-THALASSEMIA
BETA-KNOSSOS-THALASSEMIA 		1 0 1 8.3E-02 0 0
CUI: C4017510
Disease: BETA-MALAY-THALASSEMIA
BETA-MALAY-THALASSEMIA 		1 0 1 8.3E-02 0 0
CUI: C4017522
Disease: BETA-SHOWA-YAKUSHIJI THALASSEMIA
BETA-SHOWA-YAKUSHIJI THALASSEMIA 		1 0 1 8.3E-02 0 0
CUI: C4017525
Disease: BETA-PLUS-THALASSEMIA, DOMINANT
BETA-PLUS-THALASSEMIA, DOMINANT 		1 0 1 8.3E-02 0 0
CUI: C4017528
Disease: BETA-THALASSEMIA, LERMONTOV TYPE
BETA-THALASSEMIA, LERMONTOV TYPE 		1 0 1 8.3E-02 0 0
CUI: C4021641
Disease: Absence of intrinsic factor
Absence of intrinsic factor 		1 0 1 8.3E-02 0 0
CUI: C4022943
Disease: Decreased galactosylation of N-linked protein glycosylation
Decreased galactosylation of N-linked protein glycosylation 		1 0 1 8.3E-02 0 0
CUI: C4024638
Disease: Transient nephrotic syndrome
Transient nephrotic syndrome 		1 0 1 8.3E-02 0 0
CUI: C4024695
Disease: Increased red cell sickling tendency
Increased red cell sickling tendency 		1 0 1 8.3E-02 0 0
CUI: C4225242
Disease: DEHYDRATED HEREDITARY STOMATOCYTOSIS 2
DEHYDRATED HEREDITARY STOMATOCYTOSIS 2 		1 0 1 8.3E-02 0 0
CUI: C4273970
Disease: Familial pseudohyperkalemia
Familial pseudohyperkalemia 		1 0 1 8.3E-02 0 0
CUI: C4284047
Disease: HEMOGLOBIN AUBENAS PHENOTYPE
HEMOGLOBIN AUBENAS PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C4284050
Disease: HEMOGLOBIN GAMBARA PHENOTYPE
HEMOGLOBIN GAMBARA PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C4293689
Disease: Abnormal proerythroblast morphology
Abnormal proerythroblast morphology 		1 0 1 8.3E-02 0 0
CUI: C4304594
Disease: 16q24.3 microdeletion syndrome
16q24.3 microdeletion syndrome 		1 0 1 8.3E-02 0 0
CUI: C4310971
Disease: HB NIIGATA
HB NIIGATA 		1 0 1 8.3E-02 0 0
CUI: C4310973
Disease: BETA-THALASSEMIA INTERMEDIA, DOMINANT
BETA-THALASSEMIA INTERMEDIA, DOMINANT 		1 0 1 8.3E-02 0 0
CUI: C4476572
Disease: Elevated brain N-acetyl aspartate level by MRS
Elevated brain N-acetyl aspartate level by MRS 		1 0 1 8.3E-02 0 0
CUI: C4476805
Disease: Increased circulating thyroglobulin level
Increased circulating thyroglobulin level 		1 0 1 8.3E-02 0 0
CUI: C4693797
Disease: METHEMOGLOBINEMIA, BETA TYPE
METHEMOGLOBINEMIA, BETA TYPE 		1 0 1 8.3E-02 0 0