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: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 18 26 8.0E-02 1 5.0E-02
CUI: C0021933
Disease: Intussusception
Intussusception
24 1 5 7.4E-02 1 0.33
CUI: C0022665
Disease: Kidney Neoplasm
Kidney Neoplasm
295 11 9 2.7E-02 1 7.7E-02
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting
257 11 25 8.9E-02 1 7.7E-02
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
88 6387 14 0.11 1 1.6E-04
CUI: C0029927
Disease: Ovarian Cysts
Ovarian Cysts
74 3 4 3.4E-02 1 0.20
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
71 79 12 0.11 1 1.2E-02
CUI: C0042138
Disease: Uterine Neoplasms
Uterine Neoplasms
32 1 5 6.6E-02 1 0.33
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia
83 21 4 3.1E-02 1 4.3E-02
Colorectal Adenomatous Polyposis, Autosomal Recessive
1 112 1 2.0E-02 1 8.8E-03
CUI: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation
5 2 1 1.9E-02 1 0.25
CUI: C3272802
Disease: Hamartomatous polyposis
Hamartomatous polyposis
23 3 10 0.16 1 0.20
Abnormal pigmentation of the oral mucosa
1 1 1 2.0E-02 1 0.33
CUI: C4021963
Disease: Lip hyperpigmentation
Lip hyperpigmentation
1 1 1 2.0E-02 1 0.33
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 6.6E-03 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 1.6E-02 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 11 9.7E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 4 1.4E-02 0 0
CUI: C0000833
Disease: Abscess
Abscess
96 0 1 6.9E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis
161 0 2 9.6E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
46 0 1 1.1E-02 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris
94 0 1 7.0E-03 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
243 0 1 3.4E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 1.5E-02 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis
3 0 1 2.0E-02 0 0