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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious
0 4 0 0 1 8.3E-04
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia
0 1 0 0 1 8.3E-04
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma
0 1 0 0 1 8.3E-04
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 8.3E-04
CUI: C0393761
Disease: Middle insomnia
Middle insomnia
0 1 0 0 1 8.3E-04
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 8.3E-04
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0 522 0 0 1 5.8E-04
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement
0 522 0 0 1 5.8E-04
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2
0 1 0 0 1 8.3E-04
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia
152 0 1 1.2E-03 0 0
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence
151 0 1 1.2E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
127 0 1 1.3E-03 0 0
CUI: C0039070
Disease: Syncope
Syncope
119 0 1 1.3E-03 0 0
CUI: C0221002
Disease: Hyperparathyroidism, Primary
Hyperparathyroidism, Primary
115 0 1 1.3E-03 0 0
Congenital absence of kidneys syndrome
110 0 1 1.3E-03 0 0
CUI: C0020625
Disease: Hyponatremia
Hyponatremia
109 0 1 1.3E-03 0 0
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly
109 0 1 1.3E-03 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder)
109 0 1 1.3E-03 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia
109 0 1 1.3E-03 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
109 0 1 1.3E-03 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0
108 0 1 1.3E-03 0 0
CUI: C0239981
Disease: Hypoalbuminemia
Hypoalbuminemia
107 0 1 1.3E-03 0 0
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
105 0 1 1.3E-03 0 0
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
105 0 1 1.3E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin
101 0 1 1.3E-03 0 0