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: C0410192
Disease: Muscular Dystrophy, Scapulohumeral
Muscular Dystrophy, Scapulohumeral
3 0 2 0.33 0 0
CUI: C0266798
Disease: Compression of umbilical cord
Compression of umbilical cord
5 0 2 0.25 0 0
CUI: C0085222
Disease: Psoas Abscess
Psoas Abscess
1 0 1 0.20 0 0
CUI: C0270679
Disease: Brain stem herniation
Brain stem herniation
1 0 1 0.20 0 0
CUI: C0270771
Disease: Syringobulbia
Syringobulbia
1 0 1 0.20 0 0
Childhood L2 Acute Lymphoblastic Leukemia
1 0 1 0.20 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac
1 0 1 0.20 0 0
CUI: C1282310
Disease: Intermittent pain
Intermittent pain
1 0 1 0.20 0 0
CUI: C1334377
Disease: Laryngeal Sarcoma
Laryngeal Sarcoma
1 0 1 0.20 0 0
CUI: C1367539
Disease: Giant cell angiofibroma
Giant cell angiofibroma
1 0 1 0.20 0 0
Acute Hemolytic Transfusion Reaction
1 0 1 0.20 0 0
Facioscapulohumeral muscular dystrophy 1a
7 0 2 0.20 0 0
Myopathy, Hyaline Body, Autosomal Recessive
1 0 1 0.20 0 0
CUI: C2936171
Disease: Familial Ebstein's Anomaly
Familial Ebstein's Anomaly
1 0 1 0.20 0 0
CUI: C3150690
Disease: LEFT VENTRICULAR NONCOMPACTION 5
LEFT VENTRICULAR NONCOMPACTION 5
1 0 1 0.20 0 0
CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC
1 0 1 0.20 0 0
CUI: C4021811
Disease: Abnormality of the midface
Abnormality of the midface
1 0 1 0.20 0 0
CUI: C4023127
Disease: Toe extensor amyotrophy
Toe extensor amyotrophy
1 0 1 0.20 0 0
CUI: C4023292
Disease: Imperforate tricuspid valve
Imperforate tricuspid valve
1 0 1 0.20 0 0
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
1 0 1 0.20 0 0
CUI: C0232492
Disease: Upper abdominal pain
Upper abdominal pain
2 0 1 0.17 0 0
CUI: C0265740
Disease: Arrhinia
Arrhinia
2 0 1 0.17 0 0
Prolapsed thoracic intervertebral disc
2 0 1 0.17 0 0
CUI: C0520962
Disease: Localized pain
Localized pain
2 0 1 0.17 0 0
CUI: C0581321
Disease: Vertebral osteoporosis
Vertebral osteoporosis
2 0 1 0.17 0 0