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: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage 		50 0 3 4.1E-02 0 0
CUI: C2931171
Disease: Juvenile pauciarticular chronic arthritis
Juvenile pauciarticular chronic arthritis 		26 0 2 4.0E-02 0 0
CUI: C3890205
Disease: Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative 		26 0 2 4.0E-02 0 0
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		135 624 6 3.9E-02 8 1.2E-02
CUI: C0152008
Disease: Vulvovaginal disease
Vulvovaginal disease 		1 0 1 3.8E-02 0 0
CUI: C0232495
Disease: Lower abdominal pain
Lower abdominal pain 		1 0 1 3.8E-02 0 0
CUI: C0339434
Disease: Choroidal effusion
Choroidal effusion 		1 0 1 3.8E-02 0 0
CUI: C0751079
Disease: Diplopia, Vertical
Diplopia, Vertical 		1 0 1 3.8E-02 0 0
CUI: C0864813
Disease: Sporothrix schenckii Infection
Sporothrix schenckii Infection 		1 0 1 3.8E-02 0 0
CUI: C1835697
Disease: Keratitis Fugax Hereditaria
Keratitis Fugax Hereditaria 		1 0 1 3.8E-02 0 0
CUI: C1859970
Disease: Hypodysfibrinogenemia, Congenital
Hypodysfibrinogenemia, Congenital 		1 0 1 3.8E-02 0 0
CUI: C1969893
Disease: Mental Retardation, Fra12a Type
Mental Retardation, Fra12a Type 		1 0 1 3.8E-02 0 0
CUI: C3150989
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q 		1 0 1 3.8E-02 0 0
CUI: C3540094
Disease: INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 		1 1 1 3.8E-02 1 1.6E-02
CUI: C3553493
Disease: SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 		1 1 1 3.8E-02 1 1.6E-02
CUI: C3714958
Disease: PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO
PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 3.8E-02 0 0
CUI: C4016070
Disease: Fibrinogen dusart phenotype
Fibrinogen dusart phenotype 		1 0 1 3.8E-02 0 0
CUI: C4016097
Disease: FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE
FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE 		1 0 1 3.8E-02 0 0
CUI: C4072902
Disease: Reduced muscle carnitine level
Reduced muscle carnitine level 		1 0 1 3.8E-02 0 0
CUI: C4073182
Disease: Decreased carnitine level in liver
Decreased carnitine level in liver 		1 0 1 3.8E-02 0 0
CUI: C4073207
Disease: Bilateral facial muscle weakness
Bilateral facial muscle weakness 		1 0 1 3.8E-02 0 0
CUI: C4225309
Disease: EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY
EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY 		1 0 1 3.8E-02 0 0
CUI: C4477031
Disease: Axial muscle atrophy
Axial muscle atrophy 		1 0 1 3.8E-02 0 0
CUI: C4521680
Disease: DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION
DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION 		1 0 1 3.8E-02 0 0
CUI: C4316812
Disease: Fibrinogen Deficiency
Fibrinogen Deficiency 		56 0 3 3.8E-02 0 0