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: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.5E-02
CUI: C0262565
Disease: Anteroseptal Myocardial Infarction
Anteroseptal Myocardial Infarction
0 1 0 0 1 1.5E-02
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 1.5E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 1 1.4E-02
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant
0 2 0 0 2 2.9E-02
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA
0 1 0 0 1 1.5E-02
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement
0 51 0 0 1 8.5E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 1.5E-02
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement
0 51 0 0 1 8.5E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.5E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.5E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 1.4E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 1.4E-02
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
172 0 1 1.8E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 1.8E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
166 0 1 1.8E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
166 0 1 1.8E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
166 0 1 1.8E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression
165 0 1 1.8E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
165 0 1 1.8E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria
127 0 1 1.9E-03 0 0
CUI: C0476254
Disease: Dyslexia
Dyslexia
118 0 1 1.9E-03 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities
115 0 1 2.0E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness
112 0 1 2.0E-03 0 0
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly
109 0 1 2.0E-03 0 0