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: C2676078
Disease: WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1
WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1 		2 0 2 0.40 0 0
CUI: C4017326
Disease: DUFFY BLOOD GROUP SYSTEM, FY(a-b-) PHENOTYPE
DUFFY BLOOD GROUP SYSTEM, FY(a-b-) PHENOTYPE 		2 0 2 0.40 0 0
CUI: C4017327
Disease: DUFFY BLOOD GROUP SYSTEM, FY(bwk) PHENOTYPE
DUFFY BLOOD GROUP SYSTEM, FY(bwk) PHENOTYPE 		2 0 2 0.40 0 0
CUI: C1334682
Disease: Mediastinal teratoma
Mediastinal teratoma 		1 0 1 0.20 0 0
CUI: C0042251
Disease: Vaginal Diseases
Vaginal Diseases 		2 0 1 0.17 0 0
CUI: C2931185
Disease: Neonatal herpes
Neonatal herpes 		2 0 1 0.17 0 0
CUI: C4310728
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 5
SEIZURES, BENIGN FAMILIAL INFANTILE, 5 		2 0 1 0.17 0 0
CUI: C1837649
Disease: Impaired ability to form peer relationships
Impaired ability to form peer relationships 		3 0 1 0.14 0 0
CUI: C0403654
Disease: Bladder outflow obstruction
Bladder outflow obstruction 		5 0 1 0.11 0 0
CUI: C1837650
Disease: Lack of spontaneous play
Lack of spontaneous play 		5 0 1 0.11 0 0
CUI: C1837653
Disease: Inflexible adherence to routines or rituals
Inflexible adherence to routines or rituals 		5 0 1 0.11 0 0
CUI: C2698399
Disease: Myeloperoxidase Measurement
Myeloperoxidase Measurement 		15 0 2 0.11 0 0
CUI: C0019345
Disease: Herpes Labialis
Herpes Labialis 		6 0 1 1.0E-01 0 0
CUI: C0270851
Disease: Benign neonatal epilepsy
Benign neonatal epilepsy 		6 0 1 1.0E-01 0 0
CUI: C0270765
Disease: Myelopathic Muscular Atrophy
Myelopathic Muscular Atrophy 		7 0 1 9.1E-02 0 0
CUI: C1318711
Disease: Herpes simplex type 1 infection
Herpes simplex type 1 infection 		7 0 1 9.1E-02 0 0
CUI: C0877243
Disease: Increased serum serotonin
Increased serum serotonin 		8 0 1 8.3E-02 0 0
CUI: C4021798
Disease: Impaired use of nonverbal behaviors
Impaired use of nonverbal behaviors 		8 0 1 8.3E-02 0 0
CUI: C0280131
Disease: Ovarian Teratoma
Ovarian Teratoma 		9 0 1 7.7E-02 0 0
CUI: C1274323
Disease: Recurrent genital herpes simplex
Recurrent genital herpes simplex 		9 0 1 7.7E-02 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 1 7.7E-02 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 1 7.7E-02 0 0
CUI: C4024957
Disease: Proximal spinal muscular atrophy
Proximal spinal muscular atrophy 		10 0 1 7.1E-02 0 0
CUI: C1847164
Disease: Morning myoclonic jerks
Morning myoclonic jerks 		11 0 1 6.7E-02 0 0
CUI: C3494976
Disease: Migrating partial seizures in infancy
Migrating partial seizures in infancy 		11 0 1 6.7E-02 0 0