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: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome
0 3 0 0 1 2.1E-02
CUI: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic
0 1 0 0 1 2.2E-02
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
0 59 0 0 1 9.6E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 1.9E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 1 2.1E-02
CUI: C0751007
Disease: Intracranial Atherosclerosis
Intracranial Atherosclerosis
0 2 0 0 1 2.1E-02
CUI: C0865791
Disease: Obstructive bronchitis
Obstructive bronchitis
0 1 0 0 1 2.2E-02
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7
0 1 0 0 1 2.2E-02
INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
0 1 0 0 1 2.2E-02
SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
0 1 0 0 1 2.2E-02
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 6.9E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 2.6E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 6.9E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 7.0E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 7.3E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 6.6E-03 0 0
Acute and subacute liver necrosis (disorder)
6 0 1 7.2E-03 0 0
Acute vascular insufficiency of intestine (disorder)
8 0 1 7.1E-03 0 0
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma
11 0 1 7.0E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions
3 0 1 7.4E-03 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic
17 0 1 6.7E-03 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms
23 0 1 6.5E-03 0 0
CUI: C0001818
Disease: Agoraphobia
Agoraphobia
29 0 1 6.2E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 5.6E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria
13 0 1 6.9E-03 0 0