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: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		147 526 64 0.43 90 0.17
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		147 526 64 0.43 90 0.17
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		147 526 64 0.43 90 0.17
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		149 527 64 0.43 90 0.17
CUI: C1865027
Disease: Hypoplastic iliac wing
Hypoplastic iliac wing 		22 0 3 3.6E-02 0 0
CUI: C4479577
Disease: NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2
NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2 		2 0 2 3.1E-02 0 0
CUI: C0221263
Disease: Cafe-au-Lait Spots
Cafe-au-Lait Spots 		74 0 4 3.0E-02 0 0
CUI: C0425772
Disease: Premature development of the breasts
Premature development of the breasts 		7 0 2 2.9E-02 0 0
CUI: C0206739
Disease: Epithelioid and spindle cell nevus
Epithelioid and spindle cell nevus 		21 0 2 2.4E-02 0 0
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 0 2 2.4E-02 0 0
CUI: C0268079
Disease: Hyperphosphaturia
Hyperphosphaturia 		25 0 2 2.3E-02 0 0
CUI: C0080174
Disease: Spina Bifida Occulta
Spina Bifida Occulta 		76 0 3 2.2E-02 0 0
CUI: C0338113
Disease: Uterine Corpus Sarcoma
Uterine Corpus Sarcoma 		30 0 2 2.2E-02 0 0
CUI: C2825306
Disease: Treatment related leukaemia
Treatment related leukaemia 		30 0 2 2.2E-02 0 0
CUI: C0024302
Disease: Reticulosarcoma
Reticulosarcoma 		80 0 3 2.1E-02 0 0
CUI: C2697636
Disease: Hyperdiploid B Acute Lymphoblastic Leukemia
Hyperdiploid B Acute Lymphoblastic Leukemia 		32 0 2 2.1E-02 0 0
CUI: C1857042
Disease: Sparse scalp hair
Sparse scalp hair 		85 0 3 2.0E-02 0 0
CUI: C1837732
Disease: Thickened helices
Thickened helices 		37 0 2 2.0E-02 0 0
CUI: C4551560
Disease: Truncal obesity
Truncal obesity 		38 0 2 2.0E-02 0 0
CUI: C0238288
Disease: Muscular Dystrophy, Facioscapulohumeral
Muscular Dystrophy, Facioscapulohumeral 		143 0 4 2.0E-02 0 0
CUI: C1398312
Disease: Narrow palate
Narrow palate 		40 0 2 1.9E-02 0 0
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure 		40 0 2 1.9E-02 0 0
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		41 0 2 1.9E-02 0 0
CUI: C0238207
Disease: Ectopic kidney
Ectopic kidney 		41 0 2 1.9E-02 0 0
CUI: C0750929
Disease: Arnold-Chiari Malformation, Type I
Arnold-Chiari Malformation, Type I 		41 0 2 1.9E-02 0 0