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: C0220668
Disease: Congenital contractural arachnodactyly
Congenital contractural arachnodactyly 		0 48 0 0 1 5.3E-03
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
Infection caused by Helicobacter pylori 		0 56 0 0 1 5.1E-03
CUI: C1536220
Disease: ST segment elevation myocardial infarction
ST segment elevation myocardial infarction 		0 16 0 0 1 6.3E-03
CUI: C3812686
Disease: Interleukin 1 Receptor Antagonist Measurement
Interleukin 1 Receptor Antagonist Measurement 		0 11 0 0 1 6.5E-03
CUI: C4699508
Disease: Cardioembolism (high-risk/medium-risk)
Cardioembolism (high-risk/medium-risk) 		0 4 0 0 2 1.4E-02
CUI: C0152008
Disease: Vulvovaginal disease
Vulvovaginal disease 		1 0 1 1.8E-02 0 0
CUI: C0202363
Disease: Cotinine measurement
Cotinine measurement 		1 0 1 1.8E-02 0 0
CUI: C0232495
Disease: Lower abdominal pain
Lower abdominal pain 		1 0 1 1.8E-02 0 0
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis 		1 0 1 1.8E-02 0 0
CUI: C0265257
Disease: Genee-Wiedemann syndrome
Genee-Wiedemann syndrome 		1 0 1 1.8E-02 0 0
CUI: C0339434
Disease: Choroidal effusion
Choroidal effusion 		1 0 1 1.8E-02 0 0
CUI: C0751079
Disease: Diplopia, Vertical
Diplopia, Vertical 		1 0 1 1.8E-02 0 0
CUI: C0751437
Disease: Adenohypophyseal Diseases
Adenohypophyseal Diseases 		1 0 1 1.8E-02 0 0
CUI: C0751438
Disease: Posterior pituitary disease
Posterior pituitary disease 		1 0 1 1.8E-02 0 0
CUI: C0858233
Disease: Stridor, Congenital
Stridor, Congenital 		1 0 1 1.8E-02 0 0
CUI: C0863188
Disease: Stage III Carcinoma of Stomach
Stage III Carcinoma of Stomach 		1 0 1 1.8E-02 0 0
CUI: C0864813
Disease: Sporothrix schenckii Infection
Sporothrix schenckii Infection 		1 0 1 1.8E-02 0 0
CUI: C1835697
Disease: Keratitis Fugax Hereditaria
Keratitis Fugax Hereditaria 		1 0 1 1.8E-02 0 0
CUI: C1849706
Disease: Midgut malrotation
Midgut malrotation 		1 0 1 1.8E-02 0 0
CUI: C1859970
Disease: Hypodysfibrinogenemia, Congenital
Hypodysfibrinogenemia, Congenital 		1 0 1 1.8E-02 0 0
CUI: C1866933
Disease: Structural brain abnormalities
Structural brain abnormalities 		1 0 1 1.8E-02 0 0
CUI: C1969893
Disease: Mental Retardation, Fra12a Type
Mental Retardation, Fra12a Type 		1 0 1 1.8E-02 0 0
CUI: C2697767
Disease: Interleukin 19 Measurement
Interleukin 19 Measurement 		1 1 1 1.8E-02 1 7.0E-03
CUI: C3149907
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13 		1 0 1 1.8E-02 0 0
CUI: C3150989
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q 		1 0 1 1.8E-02 0 0