Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Osteomyelitis due to Staphylococcus aureus
1 0 1 1.00 0 0
CUI: C0262585
Disease: ONYCHOPATHY
ONYCHOPATHY
2 0 1 0.50 0 0
CUI: C4024843
Disease: Late onset atopic dermatitis
Late onset atopic dermatitis
2 0 1 0.50 0 0
CUI: C1868833
Disease: Bronchial wall thickening
Bronchial wall thickening
5 0 1 0.20 0 0
CUI: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome
6 0 1 0.17 0 0
CUI: C3828464
Disease: Proneural Glioblastoma
Proneural Glioblastoma
7 0 1 0.14 0 0
CUI: C3875265
Disease: Febrile urinary tract infection
Febrile urinary tract infection
8 0 1 0.12 0 0
CUI: C4324721
Disease: Radiologically isolated syndrome
Radiologically isolated syndrome
8 0 1 0.12 0 0
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency
10 0 1 1.0E-01 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis
11 0 1 9.1E-02 0 0
CUI: C0027562
Disease: Negativism
Negativism
12 0 1 8.3E-02 0 0
CUI: C0154822
Disease: Serous retinal detachment
Serous retinal detachment
12 0 1 8.3E-02 0 0
CUI: C0272236
Disease: Hyperimmunoglobulin M syndrome
Hyperimmunoglobulin M syndrome
12 0 1 8.3E-02 0 0
CUI: C0032310
Disease: Pneumonia, Viral
Pneumonia, Viral
13 0 1 7.7E-02 0 0
CUI: C1112433
Disease: Thromboembolic stroke
Thromboembolic stroke
13 0 1 7.7E-02 0 0
Social and occupational deterioration
13 0 1 7.7E-02 0 0
CUI: C3805054
Disease: Prodromal Alzheimer's disease
Prodromal Alzheimer's disease
13 0 1 7.7E-02 0 0
CUI: C0340569
Disease: Internal Carotid Artery Stenosis
Internal Carotid Artery Stenosis
15 0 1 6.7E-02 0 0
CUI: C3825816
Disease: Pneumonia in children
Pneumonia in children
15 0 1 6.7E-02 0 0
CUI: C0543698
Disease: Hypersensitive syndrome
Hypersensitive syndrome
17 0 1 5.9E-02 0 0
Acute ST segment elevation myocardial infarction (disorder)
17 0 1 5.9E-02 0 0
CUI: C4739246
Disease: Apnea+hypopnea
Apnea+hypopnea
17 0 1 5.9E-02 0 0
CUI: C0428974
Disease: Supraventricular arrhythmia
Supraventricular arrhythmia
19 0 1 5.3E-02 0 0
PREMATURE CHROMATID SEPARATION TRAIT
19 0 1 5.3E-02 0 0
Hantavirus infection in conditions classified elsewhere and of unspecified site
21 0 1 4.8E-02 0 0