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: C1281440
Disease: Familial obesity
Familial obesity
0 3 0 0 2 1.1E-02
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
Alzheimer disease, familial, type 3
0 124 0 0 1 3.3E-03
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity
0 3 0 0 2 1.1E-02
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth
0 2 0 0 1 5.4E-03
CUI: C0004669
Disease: Bacteroides Infections
Bacteroides Infections
1 0 1 1.4E-02 0 0
CUI: C0016724
Disease: Froehlich's Syndrome
Froehlich's Syndrome
1 0 1 1.4E-02 0 0
CUI: C0024967
Disease: Maximal Voluntary Ventilation
Maximal Voluntary Ventilation
1 0 1 1.4E-02 0 0
CUI: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis
1 0 1 1.4E-02 0 0
CUI: C0153661
Disease: Malignant neoplasm of thorax
Malignant neoplasm of thorax
1 0 1 1.4E-02 0 0
CUI: C0267924
Disease: Suppurative cholangitis
Suppurative cholangitis
1 0 1 1.4E-02 0 0
CUI: C0271651
Disease: Impaired glucose tolerance in obese
Impaired glucose tolerance in obese
1 0 1 1.4E-02 0 0
CUI: C0344688
Disease: Patent Ductus Venosus
Patent Ductus Venosus
1 0 1 1.4E-02 0 0
CUI: C0451818
Disease: Dietary zinc deficiency
Dietary zinc deficiency
1 0 1 1.4E-02 0 0
CUI: C0519095
Disease: tuberculosis chronic pulmonary
tuberculosis chronic pulmonary
1 0 1 1.4E-02 0 0
CUI: C1334768
Disease: Minor Salivary Gland Adenocarcinoma
Minor Salivary Gland Adenocarcinoma
1 0 1 1.4E-02 0 0
Polymorphous low grade adenocarcinoma of salivary gland
1 0 1 1.4E-02 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF
1 0 1 1.4E-02 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF
1 0 1 1.4E-02 0 0
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
1 0 1 1.4E-02 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1
1 0 1 1.4E-02 0 0
Charcot-Marie-Tooth Disease, Recessive Intermediate A
1 0 1 1.4E-02 0 0
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
1 0 1 1.4E-02 0 0
CUI: C1856301
Disease: GSD IV, Classic Hepatic
GSD IV, Classic Hepatic
1 0 1 1.4E-02 0 0
GSD IV, Neuromuscular Form, Fatal Perinatal
1 0 1 1.4E-02 0 0
GSD IV, Neuromuscular Form, Congenital
1 0 1 1.4E-02 0 0