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: C0010403
Disease: Cryoglobulinemia
Cryoglobulinemia
0 7 0 0 1 8.7E-04
CUI: C0033923
Disease: Psychomotor Performance
Psychomotor Performance
0 1 0 0 1 8.8E-04
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency
0 1 0 0 1 8.8E-04
Heparin-induced thrombocytopenia with thrombosis
0 1 0 0 1 8.8E-04
CUI: C0523550
Disease: Catalase measurement
Catalase measurement
0 2 0 0 1 8.7E-04
CUI: C0678189
Disease: Hyperlipidemia, group A
Hyperlipidemia, group A
0 1 0 0 1 8.8E-04
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait
0 2 0 0 1 8.7E-04
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 1 8.7E-04
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 1 8.7E-04
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
0 1 0 0 1 8.8E-04
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement
0 8 0 0 1 8.7E-04
CUI: C3890352
Disease: P-Selectin Measurement
P-Selectin Measurement
0 2 0 0 1 8.7E-04
CUI: C3899405
Disease: Decreased Attention
Decreased Attention
0 3 0 0 1 8.7E-04
CUI: C4050627
Disease: Soluble P-Selectin Measurement
Soluble P-Selectin Measurement
0 3 0 0 1 8.7E-04
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 1.5E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers
160 0 1 1.6E-03 0 0
Congenital ocular coloboma (disorder)
129 0 1 1.6E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth
122 0 1 1.7E-03 0 0
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
121 0 1 1.7E-03 0 0
CUI: C0240310
Disease: Hypoplasia of the maxilla
Hypoplasia of the maxilla
113 0 1 1.7E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination
112 0 1 1.7E-03 0 0
CUI: C0023479
Disease: Acute myelomonocytic leukemia
Acute myelomonocytic leukemia
105 0 1 1.7E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures
105 0 1 1.7E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 1 1.7E-03 0 0
CUI: C1368404
Disease: Hypopharyngeal Carcinoma
Hypopharyngeal Carcinoma
103 0 1 1.7E-03 0 0