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: C0042594
Disease: Vestibular Diseases
Vestibular Diseases
10 0 1 7.7E-02 0 0
CUI: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder
10 0 1 7.7E-02 0 0
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
10 0 1 7.7E-02 0 0
CUI: C0272325
Disease: Factor 8 deficiency, acquired
Factor 8 deficiency, acquired
11 0 1 7.1E-02 0 0
CUI: C0085568
Disease: Buruli Ulcer
Buruli Ulcer
13 0 1 6.2E-02 0 0
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx
13 0 1 6.2E-02 0 0
CUI: C0276926
Disease: Schistosoma hematobium infection
Schistosoma hematobium infection
13 0 1 6.2E-02 0 0
Other specified congenital malformations of respiratory system
13 0 1 6.2E-02 0 0
CUI: C0030489
Disease: Paraproteinemias
Paraproteinemias
14 0 1 5.9E-02 0 0
CUI: C1842090
Disease: Platelet Glycoprotein IV Deficiency
Platelet Glycoprotein IV Deficiency
14 0 1 5.9E-02 0 0
CUI: C0920269
Disease: Microsatellite Instability
Microsatellite Instability
15 0 1 5.6E-02 0 0
CUI: C1721098
Disease: Replication Error Phenotype
Replication Error Phenotype
15 0 1 5.6E-02 0 0
Bronchiolitis Obliterans Organizing Pneumonia
16 0 1 5.3E-02 0 0
CUI: C0023466
Disease: Leukemia, Monocytic, Chronic
Leukemia, Monocytic, Chronic
18 0 1 4.8E-02 0 0
CUI: C0403601
Disease: Transplant glomerulopathy
Transplant glomerulopathy
19 0 1 4.5E-02 0 0
CUI: C0029607
Disease: Other emphysema
Other emphysema
20 0 1 4.3E-02 0 0
CUI: C0268790
Disease: Renal vascular disorder
Renal vascular disorder
22 0 1 4.0E-02 0 0
Transient neonatal diabetes mellitus
23 0 1 3.8E-02 0 0
CUI: C3874381
Disease: Childhood nephrotic syndrome
Childhood nephrotic syndrome
23 0 1 3.8E-02 0 0
CUI: C0235063
Disease: Respiratory Depression
Respiratory Depression
24 5 1 3.7E-02 2 0.40
CUI: C0239211
Disease: Oedema auricular
Oedema auricular
24 0 1 3.7E-02 0 0
CUI: C0598784
Disease: Dyslipoproteinemias
Dyslipoproteinemias
24 0 1 3.7E-02 0 0
CUI: C1963961
Disease: Testosterone deficiency
Testosterone deficiency
24 0 1 3.7E-02 0 0
CUI: C4025860
Disease: Hearing abnormality
Hearing abnormality
24 5 1 3.7E-02 2 0.40
CUI: C4054546
Disease: Melanocortin 4 Receptor Deficiency
Melanocortin 4 Receptor Deficiency
24 28 1 3.7E-02 2 7.1E-02