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 4.0E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.4E-02 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 2.9E-02 0 0
CUI: C3669122
Disease: 5-Alpha Reductase Deficiency
5-Alpha Reductase Deficiency
8 0 1 3.7E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 2 3.3E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 3.1E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.1E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 3 3.2E-03 0 0
CUI: C1260922
Disease: Abnormal breathing
Abnormal breathing
5 0 1 4.2E-02 0 0
Abnormal form of the vertebral bodies
89 0 1 9.3E-03 0 0
CUI: C0240083
Disease: Abnormal joint morphology
Abnormal joint morphology
6 0 1 4.0E-02 0 0
CUI: C4025745
Disease: Abnormal metatarsal morphology
Abnormal metatarsal morphology
1 0 1 5.0E-02 0 0
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology
40 0 2 3.4E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 1 1.3E-02 0 0
CUI: C4025250
Disease: Abnormal sacrum morphology
Abnormal sacrum morphology
17 0 1 2.8E-02 0 0
CUI: C4025692
Disease: Abnormality of calvarial morphology
Abnormality of calvarial morphology
8 0 1 3.7E-02 0 0
Abnormality of cardiovascular system morphology
198 0 1 4.6E-03 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability
34 0 1 1.9E-02 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology
86 0 4 3.9E-02 0 0
CUI: C4021750
Disease: Abnormality of femur morphology
Abnormality of femur morphology
33 0 2 3.9E-02 0 0
CUI: C4020971
Disease: Abnormality of lower limb joint
Abnormality of lower limb joint
1 0 1 5.0E-02 0 0
Abnormality of metabolism/homeostasis
171 0 4 2.1E-02 0 0
Abnormality of pelvic girdle bone morphology
55 0 2 2.7E-02 0 0
CUI: C4021596
Disease: Abnormality of primary teeth
Abnormality of primary teeth
1 0 1 5.0E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.3E-03 0 0