Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Functional Gastrointestinal Disorders
12 0 12 1.00 0 0
CUI: C1565321
Disease: Cholera Infantum
Cholera Infantum
12 0 12 1.00 0 0
CUI: C0024799
Disease: Marginal ulcer
Marginal ulcer
3 0 2 0.15 0 0
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer
3 0 2 0.15 0 0
CUI: C0162429
Disease: Malnutrition
Malnutrition
3 0 2 0.15 0 0
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia
4 0 2 0.14 0 0
Neural tube defect, folate-sensitive
4 0 2 0.14 0 0
CUI: C0022593
Disease: Keratosis
Keratosis
5 0 2 0.13 0 0
CUI: C0022594
Disease: Keratosis Blennorrhagica
Keratosis Blennorrhagica
5 0 2 0.13 0 0
CUI: C0086501
Disease: Keratoma
Keratoma
5 0 2 0.13 0 0
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
8 0 2 0.11 0 0
CUI: C0023530
Disease: Leukopenia
Leukopenia
8 0 2 0.11 0 0
Inflammatory disease of mucous membrane
8 0 2 0.11 0 0
CUI: C1306571
Disease: Hepatic Insufficiency
Hepatic Insufficiency
9 0 2 0.11 0 0
CUI: C0242488
Disease: Acute Lung Injury
Acute Lung Injury
22 0 3 9.7E-02 0 0
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
11 0 2 9.5E-02 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
1 0 1 8.3E-02 0 0
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases
1 0 1 8.3E-02 0 0
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
1 0 1 8.3E-02 0 0
CUI: C0007166
Disease: Low Cardiac Output
Low Cardiac Output
1 0 1 8.3E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
1 0 1 8.3E-02 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden
1 0 1 8.3E-02 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis
1 0 1 8.3E-02 0 0
CUI: C0015967
Disease: Fever
Fever
27 0 3 8.3E-02 0 0
CUI: C0019572
Disease: Hirsutism
Hirsutism
1 0 1 8.3E-02 0 0