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: C1622502
Disease: Portal cirrhosis
Portal cirrhosis
4 0 1 1.0E-01 0 0
CUI: C0024248
Disease: Lymphocele
Lymphocele
5 0 1 9.1E-02 0 0
Gamma glutamyl transferase measurement
5 7 1 9.1E-02 1 6.2E-02
CUI: C0344386
Disease: Schistocytosis
Schistocytosis
5 0 1 9.1E-02 0 0
CUI: C0398777
Disease: Complement Factor H Deficiency
Complement Factor H Deficiency
5 0 1 9.1E-02 0 0
Familial Thrombotic Thrombocytopenic Purpura
5 0 1 9.1E-02 0 0
CUI: C2697760
Disease: Interleukin 12 Measurement
Interleukin 12 Measurement
5 0 1 9.1E-02 0 0
CUI: C2825877
Disease: Interferon Gamma Measurement
Interferon Gamma Measurement
5 0 1 9.1E-02 0 0
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
42 79 4 8.9E-02 6 7.2E-02
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility
6 0 1 8.3E-02 0 0
CUI: C0235299
Disease: Right upper quadrant pain
Right upper quadrant pain
6 0 1 8.3E-02 0 0
CUI: C1867396
Disease: RADIAL-RENAL SYNDROME
RADIAL-RENAL SYNDROME
6 0 1 8.3E-02 0 0
CUI: C2242816
Disease: Chronic secretory otitis media
Chronic secretory otitis media
6 0 1 8.3E-02 0 0
CUI: C4476732
Disease: Endocapillary hypercellularity
Endocapillary hypercellularity
6 0 1 8.3E-02 0 0
CUI: C0017927
Disease: Glycogen Storage Disease Type VIII
Glycogen Storage Disease Type VIII
7 0 1 7.7E-02 0 0
CUI: C0027932
Disease: Neurotic Disorders
Neurotic Disorders
7 0 1 7.7E-02 0 0
CUI: C0032176
Disease: Platelet aggregation
Platelet aggregation
7 0 1 7.7E-02 0 0
CUI: C0042998
Disease: Vulvovaginitis
Vulvovaginitis
7 0 1 7.7E-02 0 0
succinic semialdehyde dehydrogenase deficiency
7 0 1 7.7E-02 0 0
Viral gastroenteritis due to Rotavirus
7 0 1 7.7E-02 0 0
CUI: C0600502
Disease: Vascular Hemostatic Disorders
Vascular Hemostatic Disorders
7 0 1 7.7E-02 0 0
POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA
7 0 1 7.7E-02 0 0
Tricho-dento-osseous syndrome (disorder)
8 0 1 7.1E-02 0 0
CUI: C1282971
Disease: von Willebrand Disease, Type 2B
von Willebrand Disease, Type 2B
8 0 1 7.1E-02 0 0
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement
23 33 2 7.1E-02 1 2.4E-02