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: C0521668
Disease: Primary Thunderclap Headache
Primary Thunderclap Headache
1 0 1 1.00 0 0
CUI: C0685661
Disease: Congenital anomaly of ischium
Congenital anomaly of ischium
1 0 1 1.00 0 0
Soft tissue swelling of interphalangeal joints
2 0 1 0.50 0 0
CUI: C4023353
Disease: Abnormality of coordination
Abnormality of coordination
2 0 1 0.50 0 0
Dense calcifications in the cerebellar dentate nucleus
3 0 1 0.33 0 0
Calcification of the small brain vessels
3 0 1 0.33 0 0
CUI: C0236000
Disease: Jaw pain
Jaw pain
6 0 1 0.17 0 0
Idiopathic basal ganglia calcification 1
6 0 1 0.17 0 0
CUI: C0428465
Disease: Serum lipids high (finding)
Serum lipids high (finding)
7 0 1 0.14 0 0
CUI: C0423361
Disease: Posterior Vitreous Detachment
Posterior Vitreous Detachment
9 0 1 0.11 0 0
CUI: C0393590
Disease: Fahr's syndrome (disorder)
Fahr's syndrome (disorder)
10 0 1 1.0E-01 0 0
CUI: C0231557
Disease: Abnormal bone formation
Abnormal bone formation
12 0 1 8.3E-02 0 0
CUI: C0750951
Disease: Lenticulostriate Disorders
Lenticulostriate Disorders
12 0 1 8.3E-02 0 0
Placental abnormalities (excl neoplasms)
12 0 1 8.3E-02 0 0
Primary familial brain calcification
12 0 1 8.3E-02 0 0
CUI: C0240341
Disease: Micrographia
Micrographia
14 0 1 7.1E-02 0 0
CUI: C0854107
Disease: Subcutaneous hemorrhage
Subcutaneous hemorrhage
16 0 1 6.2E-02 0 0
CUI: C1854489
Disease: Limb dysmetria
Limb dysmetria
16 0 1 6.2E-02 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases
19 0 1 5.3E-02 0 0
CUI: C0085610
Disease: Sinus bradycardia
Sinus bradycardia
22 0 1 4.5E-02 0 0
CUI: C1389280
Disease: Basal ganglia calcification
Basal ganglia calcification
22 0 1 4.5E-02 0 0
CUI: C0015371
Disease: Extrapyramidal Disorders
Extrapyramidal Disorders
27 0 1 3.7E-02 0 0
CUI: C2673700
Disease: Brisk reflexes
Brisk reflexes
31 0 1 3.2E-02 0 0
CUI: C0151480
Disease: Anti-nuclear factor positive
Anti-nuclear factor positive
35 0 1 2.9E-02 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly
35 0 1 2.9E-02 0 0