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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic
0 1 0 0 1 0.33
CUI: C0268790
Disease: Renal vascular disorder
Renal vascular disorder
0 6 0 0 1 0.12
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 0.67
CUI: C0000846
Disease: Agenesis
Agenesis
161 0 1 5.5E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 3.2E-02 0 0
Acute and subacute liver necrosis (disorder)
6 0 1 3.8E-02 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis
11 3 1 3.2E-02 2 0.50
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis
9 0 1 3.4E-02 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease
111 0 1 7.6E-03 0 0
CUI: C0001510
Disease: Postoperative adhesion
Postoperative adhesion
9 0 1 3.4E-02 0 0
CUI: C0001618
Disease: Tumors of Adrenal Cortex
Tumors of Adrenal Cortex
74 0 1 1.1E-02 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases
9 0 1 3.4E-02 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
90 0 1 9.1E-03 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms
94 0 1 8.8E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
87 0 1 9.3E-03 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic
17 0 1 2.7E-02 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms
23 0 1 2.3E-02 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related
89 0 1 9.2E-03 0 0
CUI: C0001818
Disease: Agoraphobia
Agoraphobia
29 0 1 2.0E-02 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
55 0 1 1.3E-02 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria
76 0 1 1.0E-02 0 0
CUI: C0001969
Disease: Alcoholic Intoxication
Alcoholic Intoxication
52 0 1 1.4E-02 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis
13 0 1 3.0E-02 0 0
CUI: C0002448
Disease: Ameloblastoma
Ameloblastoma
174 0 1 5.2E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity
14 0 1 2.9E-02 0 0