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: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 1 5.0E-02 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 1 2.3E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 2 3.9E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 1.8E-02 0 0
CUI: C0243001
Disease: Abdominal Abscess
Abdominal Abscess
4 0 1 5.6E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 3.2E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 2 3.7E-02 0 0
Abnormal atrioventricular conduction
7 0 1 4.8E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 4 4.3E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 1.1E-02 0 0
Abnormal brain FDG positron emission tomography
18 0 1 3.1E-02 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 5.6E-02 0 0
Abnormal electrophysiology of sinoatrial node origin
1 0 1 6.7E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 2.3E-02 0 0
CUI: C3280303
Disease: Abnormal hair whorl
Abnormal hair whorl
5 0 1 5.3E-02 0 0
CUI: C0241654
Disease: Abnormal heart valve morphology
Abnormal heart valve morphology
42 0 1 1.8E-02 0 0
Abnormal lower motor neuron morphology
23 0 1 2.7E-02 0 0
CUI: C4531142
Disease: Abnormal lymphocyte physiology
Abnormal lymphocyte physiology
1 0 1 6.7E-02 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology
13 0 1 3.7E-02 0 0
CUI: C4020957
Disease: Abnormal trabecular bone morphology
Abnormal trabecular bone morphology
6 0 1 5.0E-02 0 0
Abnormal upper motor neuron morphology
20 0 1 2.9E-02 0 0
Abnormality of blood and blood-forming tissues
23 0 1 2.7E-02 0 0
Abnormality of circulating leptin level
1 0 1 6.7E-02 0 0
CUI: C4025213
Disease: Abnormality of complement system
Abnormality of complement system
2 0 1 6.2E-02 0 0