Source: ALL
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: C4017091
Disease: ARYLSULFATASE A PSEUDODEFICIENCY
ARYLSULFATASE A PSEUDODEFICIENCY 		0 3 0 0 1 3.2E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.2E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 6.3E-03
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia 		59 0 1 3.8E-04 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 3.8E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 3.8E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 3.8E-04 0 0
CUI: C4021546
Disease: Abnormal mitochondria in muscle tissue
Abnormal mitochondria in muscle tissue 		39 0 1 3.8E-04 0 0
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder 		37 0 1 3.8E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy 		37 0 1 3.8E-04 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis 		35 0 1 3.9E-04 0 0
CUI: C0019553
Disease: Hip Contracture
Hip Contracture 		34 0 1 3.9E-04 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		33 0 1 3.9E-04 0 0
CUI: C1854838
Disease: Progressive neurologic deterioration
Progressive neurologic deterioration 		33 0 1 3.9E-04 0 0
CUI: C4022748
Disease: Focal T2 hyperintense brainstem lesion
Focal T2 hyperintense brainstem lesion 		33 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: C0878575
Disease: Peripheral demyelination
Peripheral demyelination 		27 0 1 3.9E-04 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 1 3.9E-04 0 0
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: C0155707
Disease: Trifascicular block
Trifascicular block 		23 0 1 3.9E-04 0 0
CUI: C0201925
Disease: Calcium measurement
Calcium measurement 		23 71 1 3.9E-04 1 2.6E-03
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding) 		23 0 1 3.9E-04 0 0