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: C0001139
Disease: Acinetobacter Infections
Acinetobacter Infections
1 0 1 2.0E-02 0 0
CUI: C0031946
Disease: Pinta
Pinta
1 0 1 2.0E-02 0 0
CUI: C0155781
Disease: Thrombosed internal hemorrhoids
Thrombosed internal hemorrhoids
1 0 1 2.0E-02 0 0
CUI: C0234175
Disease: Palmar reflex
Palmar reflex
1 0 1 2.0E-02 0 0
CUI: C0234435
Disease: Syncope, Tussive
Syncope, Tussive
1 0 1 2.0E-02 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction
1 0 1 2.0E-02 0 0
CUI: C0237811
Disease: Acute Psychotic Episode
Acute Psychotic Episode
1 0 1 2.0E-02 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure
1 0 1 2.0E-02 0 0
salivary gland squamous cell carcinoma
1 0 1 2.0E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I
1 0 1 2.0E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II
1 0 1 2.0E-02 0 0
Endometrioid adenoma, borderline malignancy
1 0 1 2.0E-02 0 0
CUI: C0334566
Disease: Ghost Cell Odontogenic Carcinoma
Ghost Cell Odontogenic Carcinoma
1 0 1 2.0E-02 0 0
CUI: C0406571
Disease: Superficial fibromatosis
Superficial fibromatosis
1 0 1 2.0E-02 0 0
Respiratory distress syndrome, children
1 0 1 2.0E-02 0 0
3-Phosphoglycerate dehydrogenase deficiency
1 0 1 2.0E-02 0 0
microcephaly-digital anomalies syndrome
1 0 1 2.0E-02 0 0
CUI: C1152136
Disease: sucrose-phosphate synthase activity
sucrose-phosphate synthase activity
1 0 1 2.0E-02 0 0
CUI: C1275420
Disease: Extra-abdominal fibromatosis
Extra-abdominal fibromatosis
1 0 1 2.0E-02 0 0
CUI: C1333117
Disease: Colorectal Tubular Adenoma
Colorectal Tubular Adenoma
1 0 1 2.0E-02 0 0
CUI: C1527225
Disease: Radiation-induced disorder
Radiation-induced disorder
1 0 1 2.0E-02 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder
1 0 1 2.0E-02 0 0
CUI: C1704219
Disease: Dentinogenic Ghost Cell Tumor
Dentinogenic Ghost Cell Tumor
1 0 1 2.0E-02 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3
1 10 1 2.0E-02 1 2.6E-02
MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
1 8 1 2.0E-02 1 2.8E-02