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: C0585475
Disease: Pilomatrix carcinoma of skin
Pilomatrix carcinoma of skin
0 3 0 0 1 1.8E-02
CUI: C4703722
Disease: Superior rectus muscle underaction
Superior rectus muscle underaction
0 1 0 0 1 1.8E-02
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 1.1E-03 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk
77 0 1 1.1E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia
75 0 1 1.1E-03 0 0
CUI: C1844813
Disease: Widely spaced teeth
Widely spaced teeth
71 0 1 1.1E-03 0 0
Abnormality of the hypothalamus-pituitary axis
70 0 1 1.1E-03 0 0
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis
69 0 1 1.1E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
67 0 1 1.1E-03 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly
67 0 1 1.1E-03 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
66 0 1 1.1E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result
65 0 1 1.1E-03 0 0
CUI: C1843921
Disease: Postural instability
Postural instability
60 0 1 1.1E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function
59 0 1 1.1E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction
57 0 1 1.1E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 0 1 1.1E-03 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy
56 0 1 1.1E-03 0 0
CUI: C0010520
Disease: Cyanosis
Cyanosis
54 0 1 1.1E-03 0 0
Serum gamma-glutamyl transferase measurement
54 0 1 1.1E-03 0 0
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement
53 0 1 1.1E-03 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement
53 0 1 1.1E-03 0 0
CUI: C1860816
Disease: Preauricular skin tag
Preauricular skin tag
53 0 1 1.1E-03 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms
53 0 1 1.1E-03 0 0
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly
51 0 1 1.1E-03 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
50 0 1 1.2E-03 0 0