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: C0342953
Disease: Organ dysfunction syndrome
Organ dysfunction syndrome
0 6 0 0 1 1.7E-02
Left ventricular systolic dysfunction
0 11 0 0 1 1.6E-02
CUI: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic
1 0 1 2.4E-02 0 0
CUI: C0037998
Disease: Splenic Infarction
Splenic Infarction
1 0 1 2.4E-02 0 0
CUI: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever
1 0 1 2.4E-02 0 0
CUI: C0155829
Disease: Enlargement of tonsil or adenoid
Enlargement of tonsil or adenoid
1 0 1 2.4E-02 0 0
CUI: C0263145
Disease: Cellulitis of abdominal wall
Cellulitis of abdominal wall
1 0 1 2.4E-02 0 0
CUI: C0265363
Disease: Urethral obstruction sequence
Urethral obstruction sequence
1 0 1 2.4E-02 0 0
CUI: C0265593
Disease: Brachymetacarpia
Brachymetacarpia
1 0 1 2.4E-02 0 0
Derangement of temporomandibular joint
1 0 1 2.4E-02 0 0
Mild steroid 21-hydroxylase deficiency
1 0 1 2.4E-02 0 0
CUI: C0276085
Disease: Ecthyma gangrenosum
Ecthyma gangrenosum
1 0 1 2.4E-02 0 0
CUI: C0277526
Disease: Dysenteric diarrhea
Dysenteric diarrhea
1 0 1 2.4E-02 0 0
Adult Acute Myeloid Leukemia in Remission
1 0 1 2.4E-02 0 0
Childhood Acute Myeloid Leukemia in Remission
1 0 1 2.4E-02 0 0
CUI: C0281952
Disease: Pseudohypothyroidism
Pseudohypothyroidism
1 0 1 2.4E-02 0 0
CUI: C0343287
Disease: Thoracic discitis
Thoracic discitis
1 0 1 2.4E-02 0 0
CUI: C0423463
Disease: Opticociliary vessels
Opticociliary vessels
1 0 1 2.4E-02 0 0
CUI: C0570855
Disease: Allergy to chlorpromazine
Allergy to chlorpromazine
1 0 1 2.4E-02 0 0
CUI: C0858906
Disease: Infection pyogenic
Infection pyogenic
1 0 1 2.4E-02 0 0
CUI: C0877058
Disease: Lymphocytic dermatitis
Lymphocytic dermatitis
1 0 1 2.4E-02 0 0
CUI: C1304408
Disease: Urticarial vasculitis
Urticarial vasculitis
1 0 1 2.4E-02 0 0
CUI: C1335381
Disease: Pericardial mesothelioma
Pericardial mesothelioma
1 0 1 2.4E-02 0 0
CUI: C1707332
Disease: Cellular Myxoma
Cellular Myxoma
1 0 1 2.4E-02 0 0
Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency
1 0 1 2.4E-02 0 0