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: C0002534
Disease: Renal Aminoacidurias
Renal Aminoacidurias
1 0 1 2.3E-02 0 0
CUI: C0003910
Disease: Articulation Disorders
Articulation Disorders
1 0 1 2.3E-02 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden
1 0 1 2.3E-02 0 0
Food poisoning caused by Vibrio parahaemolyticus
1 0 1 2.3E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers
1 0 1 2.3E-02 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe
1 0 1 2.3E-02 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle
1 0 1 2.3E-02 0 0
CUI: C0234918
Disease: Morbilliform rash
Morbilliform rash
1 0 1 2.3E-02 0 0
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction
1 0 1 2.3E-02 0 0
Disorder of phenylalanine metabolism
1 0 1 2.3E-02 0 0
CUI: C0268543
Disease: Hyperammonemia, type III
Hyperammonemia, type III
1 0 1 2.3E-02 0 0
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis
1 0 1 2.3E-02 0 0
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction
1 0 1 2.3E-02 0 0
CUI: C0345183
Disease: Congenital constriction of pylorus
Congenital constriction of pylorus
1 0 1 2.3E-02 0 0
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia
1 0 1 2.3E-02 0 0
CUI: C0406607
Disease: Insulin lipoatrophy
Insulin lipoatrophy
1 0 1 2.3E-02 0 0
Congenital malformation syndromes involving early overgrowth
1 0 1 2.3E-02 0 0
CUI: C0745868
Disease: lower extremity neuropathy
lower extremity neuropathy
1 0 1 2.3E-02 0 0
CUI: C0751549
Disease: Neurogenic Thoracic Outlet Syndrome
Neurogenic Thoracic Outlet Syndrome
1 0 1 2.3E-02 0 0
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion
1 0 1 2.3E-02 0 0
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma
1 0 1 2.3E-02 0 0
CUI: C1263739
Disease: Disorder of organic acid metabolism
Disorder of organic acid metabolism
1 0 1 2.3E-02 0 0
CUI: C1274594
Disease: Lichenoid actinic keratosis
Lichenoid actinic keratosis
1 0 1 2.3E-02 0 0
Hyper-IgD periodic fever syndrome (HIDS)
1 0 1 2.3E-02 0 0
CUI: C1302778
Disease: Congenital lymphatic malformation
Congenital lymphatic malformation
1 0 1 2.3E-02 0 0