Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Frequent episodic tension-type headache
0 1 0 0 1 1.3E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 2.6E-03
CUI: C1855672
Disease: Immotile cilia
Immotile cilia
41 0 1 3.9E-04 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness
41 0 1 3.9E-04 0 0
Impaired nasal mucociliary clearance
41 0 1 3.9E-04 0 0
Abnormal mitochondria in muscle tissue
39 0 1 3.9E-04 0 0
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
37 0 1 3.9E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy
37 0 1 3.9E-04 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 1 3.9E-04 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis
35 0 1 3.9E-04 0 0
Focal T2 hyperintense brainstem lesion
33 0 1 3.9E-04 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
32 0 1 3.9E-04 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity
29 0 1 3.9E-04 0 0
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy
29 0 1 3.9E-04 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness
28 0 1 3.9E-04 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia
26 0 1 3.9E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome
26 0 1 3.9E-04 0 0
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement
26 36 1 3.9E-04 1 1.3E-03
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding)
25 0 1 3.9E-04 0 0
CUI: C1842153
Disease: Irregular vertebral endplates
Irregular vertebral endplates
24 0 1 3.9E-04 0 0
CUI: C0201925
Disease: Calcium measurement
Calcium measurement
23 71 1 3.9E-04 1 1.2E-03
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding)
23 0 1 3.9E-04 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
23 0 1 3.9E-04 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes
23 0 1 3.9E-04 0 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting
22 0 1 3.9E-04 0 0