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: C3698348
Disease: Anti-D isoimmunization affecting pregnancy
Anti-D isoimmunization affecting pregnancy 		2 0 2 0.25 0 0
CUI: C4015919
Disease: RHD CATEGORY D-VII
RHD CATEGORY D-VII 		2 0 2 0.25 0 0
CUI: C4015920
Disease: RHD, WEAK D, TYPE I
RHD, WEAK D, TYPE I 		2 0 2 0.25 0 0
CUI: C0158962
Disease: Hemolytic disease of fetus OR newborn due to RhD isoimmunization
Hemolytic disease of fetus OR newborn due to RhD isoimmunization 		3 0 2 0.22 0 0
CUI: C0020800
Disease: Idiopathic Hypercatabolic Hypoproteinemia
Idiopathic Hypercatabolic Hypoproteinemia 		1 0 1 0.12 0 0
CUI: C0234458
Disease: Dream disorder
Dream disorder 		1 0 1 0.12 0 0
CUI: C0458118
Disease: Total body pain syndrome
Total body pain syndrome 		1 0 1 0.12 0 0
CUI: C0751868
Disease: Alcohol Withdrawal-Induced Major Motor Seizure
Alcohol Withdrawal-Induced Major Motor Seizure 		1 0 1 0.12 0 0
CUI: C0751869
Disease: Status Epilepticus, Alcohol Withdrawal-Induced
Status Epilepticus, Alcohol Withdrawal-Induced 		1 0 1 0.12 0 0
CUI: C0862953
Disease: Cholangiocarcinoma non-resectable
Cholangiocarcinoma non-resectable 		1 0 1 0.12 0 0
CUI: C1274408
Disease: Chronic plaque-like oral candidiasis
Chronic plaque-like oral candidiasis 		1 0 1 0.12 0 0
CUI: C1292231
Disease: In(Lu) phenotype (finding)
In(Lu) phenotype (finding) 		1 10 1 0.12 1 6.7E-02
CUI: C1306229
Disease: Dyschromatosis universalis
Dyschromatosis universalis 		1 0 1 0.12 0 0
CUI: C1410087
Disease: Spine stiffness
Spine stiffness 		1 0 1 0.12 0 0
CUI: C1836705
Disease: Pseudohyperkalemia, Familial, 2, due to Red Cell Leak
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak 		1 0 1 0.12 0 0
CUI: C1862229
Disease: Adult i Blood Group Phenotype
Adult i Blood Group Phenotype 		1 0 1 0.12 0 0
CUI: C3150805
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6 		1 0 1 0.12 0 0
CUI: C3549486
Disease: NOR POLYAGGLUTINATION SYNDROME
NOR POLYAGGLUTINATION SYNDROME 		1 0 1 0.12 0 0
CUI: C3805373
Disease: CATARACT 13 WITH ADULT i PHENOTYPE
CATARACT 13 WITH ADULT i PHENOTYPE 		1 0 1 0.12 0 0
CUI: C3809394
Disease: DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3 		1 0 1 0.12 0 0
CUI: C4023619
Disease: Absence of Lutheran antigen on erythrocytes
Absence of Lutheran antigen on erythrocytes 		1 0 1 0.12 0 0
CUI: C4273970
Disease: Familial pseudohyperkalemia
Familial pseudohyperkalemia 		1 0 1 0.12 0 0
CUI: C4540531
Disease: CROMER BLOOD GROUP SYSTEM, Dr(a-) PHENOTYPE
CROMER BLOOD GROUP SYSTEM, Dr(a-) PHENOTYPE 		1 0 1 0.12 0 0
CUI: C0039010
Disease: Swine Vesicular Disease
Swine Vesicular Disease 		2 0 1 0.11 0 0
CUI: C0267372
Disease: Primary intestinal lymphangiectasia
Primary intestinal lymphangiectasia 		2 0 1 0.11 0 0