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: C0740406
Disease: Incarcerated hernia
Incarcerated hernia 		1 0 1 6.7E-02 0 0
CUI: C0745868
Disease: lower extremity neuropathy
lower extremity neuropathy 		1 0 1 6.7E-02 0 0
CUI: C0751549
Disease: Neurogenic Thoracic Outlet Syndrome
Neurogenic Thoracic Outlet Syndrome 		1 0 1 6.7E-02 0 0
CUI: C0919823
Disease: Cytolytic hepatitis
Cytolytic hepatitis 		1 0 1 6.7E-02 0 0
CUI: C1263726
Disease: Sulfatiduria
Sulfatiduria 		1 0 1 6.7E-02 0 0
CUI: C1275345
Disease: Familial mastocytosis
Familial mastocytosis 		1 0 1 6.7E-02 0 0
CUI: C1328500
Disease: Intraoperative hypertension
Intraoperative hypertension 		1 0 1 6.7E-02 0 0
CUI: C1333460
Disease: Esophageal Melanoma
Esophageal Melanoma 		1 0 1 6.7E-02 0 0
CUI: C1333802
Disease: Gastrointestinal Stromal Tumor of the Gastrointestinal Tract
Gastrointestinal Stromal Tumor of the Gastrointestinal Tract 		1 0 1 6.7E-02 0 0
CUI: C1334222
Disease: Intermediate Risk Gastrointestinal Stromal Tumor
Intermediate Risk Gastrointestinal Stromal Tumor 		1 0 1 6.7E-02 0 0
CUI: C1336056
Disease: Spindle Cell Type Gastrointestinal Stromal Tumor
Spindle Cell Type Gastrointestinal Stromal Tumor 		1 0 1 6.7E-02 0 0
CUI: C1456270
Disease: Fatty acid oxidation disorder
Fatty acid oxidation disorder 		1 0 1 6.7E-02 0 0
CUI: C1541333
Disease: adult acute myeloid leukemia with inv(16)(p13;q22)
adult acute myeloid leukemia with inv(16)(p13;q22) 		1 0 1 6.7E-02 0 0
CUI: C1706192
Disease: Sulfatidosis
Sulfatidosis 		1 0 1 6.7E-02 0 0
CUI: C1833508
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET 		1 0 1 6.7E-02 0 0
CUI: C1833511
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE 		1 0 1 6.7E-02 0 0
CUI: C1833518
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL 		1 0 1 6.7E-02 0 0
CUI: C1837273
Disease: Long-chain dicarboxylic aciduria
Long-chain dicarboxylic aciduria 		1 0 1 6.7E-02 0 0
CUI: C1850722
Disease: Transient hyperlipidemia
Transient hyperlipidemia 		1 0 1 6.7E-02 0 0
CUI: C1855255
Disease: Pseudoarylsulfatase A Deficiency
Pseudoarylsulfatase A Deficiency 		1 0 1 6.7E-02 0 0
CUI: C1860081
Disease: Medium chain dicarboxylic aciduria
Medium chain dicarboxylic aciduria 		1 0 1 6.7E-02 0 0
CUI: C1881170
Disease: Inappropriate sinus tachycardia
Inappropriate sinus tachycardia 		1 0 1 6.7E-02 0 0
CUI: C1963905
Disease: Infantile free sialic acid storage disease
Infantile free sialic acid storage disease 		1 0 1 6.7E-02 0 0
CUI: C2674636
Disease: GASTROINTESTINAL STROMAL TUMOR, FAMILIAL
GASTROINTESTINAL STROMAL TUMOR, FAMILIAL 		1 0 1 6.7E-02 0 0
CUI: C2675488
Disease: Mental Retardation, Autosomal Dominant 3
Mental Retardation, Autosomal Dominant 3 		1 0 1 6.7E-02 0 0