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: C0039614
Disease: Tetanus
Tetanus 		1 0 1 2.4E-02 0 0
CUI: C0149882
Disease: Acute esophagitis
Acute esophagitis 		1 0 1 2.4E-02 0 0
CUI: C0151772
Disease: Manic psychosis
Manic psychosis 		1 0 1 2.4E-02 0 0
CUI: C0235915
Disease: Pulmonary malformation
Pulmonary malformation 		1 0 1 2.4E-02 0 0
CUI: C0333992
Disease: Acanthoma, Clear Cell
Acanthoma, Clear Cell 		1 0 1 2.4E-02 0 0
CUI: C0342278
Disease: Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 		1 0 1 2.4E-02 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 2.4E-02 0 0
CUI: C0854771
Disease: Stage I Esophageal Squamous Cell Carcinoma
Stage I Esophageal Squamous Cell Carcinoma 		1 0 1 2.4E-02 0 0
CUI: C1112473
Disease: Mast cell aggregation
Mast cell aggregation 		1 0 1 2.4E-02 0 0
CUI: C1864952
Disease: Hyperinsulinemic Hypoglycemia, Familial, 5
Hyperinsulinemic Hypoglycemia, Familial, 5 		1 0 1 2.4E-02 0 0
CUI: C1969785
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder) 		1 0 1 2.4E-02 0 0
CUI: C1997262
Disease: Hypothyroidism in pregnancy
Hypothyroidism in pregnancy 		1 1 1 2.4E-02 1 1.2E-02
CUI: C2931517
Disease: Plasmacytoma anaplastic
Plasmacytoma anaplastic 		1 0 1 2.4E-02 0 0
CUI: C3151036
Disease: CHROMOSOME 1p32-p31 DELETION SYNDROME
CHROMOSOME 1p32-p31 DELETION SYNDROME 		1 0 1 2.4E-02 0 0
CUI: C3280094
Disease: PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3 		1 0 1 2.4E-02 0 0
CUI: C3489787
Disease: Pituitary Hormone Deficiency, Combined, 3
Pituitary Hormone Deficiency, Combined, 3 		1 0 1 2.4E-02 0 0
CUI: C3495361
Disease: Gigantiform Cementoma, Familial
Gigantiform Cementoma, Familial 		1 0 1 2.4E-02 0 0
CUI: C4022967
Disease: Hypothalamic luteinizing hormone-releasing hormone deficiency
Hypothalamic luteinizing hormone-releasing hormone deficiency 		1 0 1 2.4E-02 0 0
CUI: C4024947
Disease: Symmetric lesions of the basal ganglia
Symmetric lesions of the basal ganglia 		1 0 1 2.4E-02 0 0
CUI: C4310791
Disease: STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2
STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2 		1 0 1 2.4E-02 0 0
CUI: C4310792
Disease: DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET
DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET 		1 0 1 2.4E-02 0 0
CUI: C4310808
Disease: STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1
STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1 		1 0 1 2.4E-02 0 0
CUI: C4324411
Disease: Blood type incompatibility
Blood type incompatibility 		1 0 1 2.4E-02 0 0
CUI: C4478940
Disease: BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS
BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS 		1 0 1 2.4E-02 0 0
CUI: C4531279
Disease: Striatal T2 hyperintensity
Striatal T2 hyperintensity 		1 0 1 2.4E-02 0 0