Source: INFERRED ×
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: C0014394
Disease: Enuresis
Enuresis 		0 3 0 0 1 8.3E-03
CUI: C1836696
Disease: Lower limb hyperreflexia
Lower limb hyperreflexia 		0 6 0 0 1 8.1E-03
CUI: C4023077
Disease: EEG with central focal spikes
EEG with central focal spikes 		0 2 0 0 1 8.4E-03
CUI: C4023353
Disease: Abnormality of coordination
Abnormality of coordination 		0 3 0 0 1 8.3E-03
CUI: C4025792
Disease: EEG with irregular generalized spike and wave complexes
EEG with irregular generalized spike and wave complexes 		0 1 0 0 1 8.5E-03
CUI: C4317045
Disease: Gluten intolerance
Gluten intolerance 		0 1 0 0 1 8.5E-03
CUI: C4693362
Disease: EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2
EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2 		0 6 0 0 1 8.1E-03
CUI: C0016512
Disease: Foot pain
Foot pain 		1 0 1 1.1E-02 0 0
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		1 165 1 1.1E-02 1 3.5E-03
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		1 1 1 1.1E-02 1 8.5E-03
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		1 0 1 1.1E-02 0 0
CUI: C0029877
Disease: Ear Inflammation
Ear Inflammation 		1 2 1 1.1E-02 2 1.7E-02
CUI: C0079294
Disease: Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa Dystrophica 		1 0 1 1.1E-02 0 0
CUI: C0079301
Disease: Junctional Epidermolysis Bullosa
Junctional Epidermolysis Bullosa 		1 0 1 1.1E-02 0 0
CUI: C0079474
Disease: Hallopeau-Siemens Disease
Hallopeau-Siemens Disease 		1 40 1 1.1E-02 1 6.4E-03
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 1.1E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 3 1 1.1E-02 1 8.3E-03
CUI: C0262665
Disease: Abnormal vocal cord morphology
Abnormal vocal cord morphology 		1 2 1 1.1E-02 2 1.7E-02
CUI: C0265211
Disease: Marshall-Smith syndrome
Marshall-Smith syndrome 		1 17 1 1.1E-02 1 7.5E-03
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		1 0 1 1.1E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 1.1E-02 0 0
CUI: C0268250
Disease: Gaucher Disease, Type 2 (disorder)
Gaucher Disease, Type 2 (disorder) 		1 0 1 1.1E-02 0 0
CUI: C0268251
Disease: Gaucher Disease, Type 3 (disorder)
Gaucher Disease, Type 3 (disorder) 		1 0 1 1.1E-02 0 0
CUI: C0268371
Disease: Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails 		1 0 1 1.1E-02 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 1.1E-02 0 0