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: C0236811
Disease: Chronobiology Disorders
Chronobiology Disorders
3 0 2 0.12 0 0
Psychogenic Inversion of Circadian Rhythm
3 0 2 0.12 0 0
CUI: C0201952
Disease: Chloride measurement
Chloride measurement
16 19 3 0.10 2 4.4E-02
CUI: C0813142
Disease: Circadian Rhythm Disorders
Circadian Rhythm Disorders
11 0 2 8.0E-02 0 0
CUI: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis
1 0 1 6.2E-02 0 0
CUI: C0178272
Disease: Disorder of pulmonary circulation
Disorder of pulmonary circulation
1 0 1 6.2E-02 0 0
CUI: C0264487
Disease: Chronic nonspecific lung disease
Chronic nonspecific lung disease
1 0 1 6.2E-02 0 0
CUI: C0272157
Disease: Disorder of neutrophils
Disorder of neutrophils
1 0 1 6.2E-02 0 0
CUI: C0344688
Disease: Patent Ductus Venosus
Patent Ductus Venosus
1 0 1 6.2E-02 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF
1 0 1 6.2E-02 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF
1 0 1 6.2E-02 0 0
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
1 0 1 6.2E-02 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1
1 0 1 6.2E-02 0 0
Amelogenesis Imperfecta, Hypomaturation Type, Iia3
1 0 1 6.2E-02 0 0
CUI: C2931037
Disease: Pancreatic cancer, adult
Pancreatic cancer, adult
1 0 1 6.2E-02 0 0
CUI: C3809198
Disease: PULMONARY HYPERTENSION, PRIMARY, 4
PULMONARY HYPERTENSION, PRIMARY, 4
1 0 1 6.2E-02 0 0
CUI: C3839047
Disease: Severe dry skin
Severe dry skin
1 0 1 6.2E-02 0 0
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
1 0 1 6.2E-02 0 0
CUI: C4021748
Disease: Abnormal B cell morphology
Abnormal B cell morphology
1 0 1 6.2E-02 0 0
Increased carotid artery intimal medial thickness
1 0 1 6.2E-02 0 0
CUI: C4023540
Disease: Hypomature dental enamel
Hypomature dental enamel
1 0 1 6.2E-02 0 0
CUI: C4225166
Disease: NEPHROTIC SYNDROME, TYPE 12
NEPHROTIC SYNDROME, TYPE 12
1 0 1 6.2E-02 0 0
CUI: C4476942
Disease: Impaired feeding ability
Impaired feeding ability
1 0 1 6.2E-02 0 0
CUI: C4748517
Disease: DIARRHEA 9
DIARRHEA 9
1 0 1 6.2E-02 0 0
VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION
1 0 1 6.2E-02 0 0