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: C0155866
Disease: Inhalational anthrax
Inhalational anthrax 		2 0 1 0.33 0 0
CUI: C0238434
Disease: Epidural Abscess, Spinal
Epidural Abscess, Spinal 		2 0 1 0.33 0 0
CUI: C0398703
Disease: Immunoglobulin G3 deficiency
Immunoglobulin G3 deficiency 		2 0 1 0.33 0 0
CUI: C0398704
Disease: Immunoglobulin G4 deficiency
Immunoglobulin G4 deficiency 		2 0 1 0.33 0 0
CUI: C4021165
Disease: Abnormality of long bone morphology
Abnormality of long bone morphology 		3 0 1 0.25 0 0
CUI: C4023052
Disease: Ubiquitin-positive cerebral inclusion bodies
Ubiquitin-positive cerebral inclusion bodies 		3 0 1 0.25 0 0
CUI: C0149514
Disease: Acute bronchitis
Acute bronchitis 		4 0 1 0.20 0 0
CUI: C0272118
Disease: Warm autoimmune hemolytic anemia
Warm autoimmune hemolytic anemia 		4 0 1 0.20 0 0
CUI: C0398701
Disease: Immunoglobulin G2 deficiency
Immunoglobulin G2 deficiency 		4 0 1 0.20 0 0
CUI: C1291230
Disease: 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
3-Hydroxyacyl-CoA Dehydrogenase Deficiency 		4 0 1 0.20 0 0
CUI: C4025347
Disease: Weakness of muscles of respiration
Weakness of muscles of respiration 		4 0 1 0.20 0 0
CUI: C0013882
Disease: Elephantiasis
Elephantiasis 		6 0 1 0.14 0 0
CUI: C0018852
Disease: Heavy Chain Disease
Heavy Chain Disease 		6 0 1 0.14 0 0
CUI: C0038463
Disease: Strongyloidiasis
Strongyloidiasis 		6 0 1 0.14 0 0
CUI: C4054543
Disease: Membranous Lupus Nephritis
Membranous Lupus Nephritis 		6 0 1 0.14 0 0
CUI: C4025692
Disease: Abnormality of calvarial morphology
Abnormality of calvarial morphology 		8 0 1 0.11 0 0
CUI: C1274323
Disease: Recurrent genital herpes simplex
Recurrent genital herpes simplex 		9 0 1 1.0E-01 0 0
CUI: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder 		10 0 1 9.1E-02 0 0
CUI: C1845052
Disease: AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1 		10 0 1 9.1E-02 0 0
CUI: C1863351
Disease: Calvarial hyperostosis
Calvarial hyperostosis 		10 0 1 9.1E-02 0 0
CUI: C0272325
Disease: Factor 8 deficiency, acquired
Factor 8 deficiency, acquired 		11 0 1 8.3E-02 0 0
CUI: C0276926
Disease: Schistosoma hematobium infection
Schistosoma hematobium infection 		13 0 1 7.1E-02 0 0
CUI: C1839042
Disease: Upper motor neuron dysfunction
Upper motor neuron dysfunction 		16 0 1 5.9E-02 0 0
CUI: C4021082
Disease: Fatty replacement of skeletal muscle
Fatty replacement of skeletal muscle 		17 0 1 5.6E-02 0 0
CUI: C4025614
Disease: EMG: chronic denervation signs
EMG: chronic denervation signs 		18 0 1 5.3E-02 0 0