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: C1851943
Disease: DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT (disorder)
DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT (disorder) 		2 0 1 0.11 0 0
CUI: C1860315
Disease: Whispering dysphonia, hereditary
Whispering dysphonia, hereditary 		2 0 1 0.11 0 0
CUI: C1864002
Disease: GRACILE SYNDROME (disorder)
GRACILE SYNDROME (disorder) 		2 0 1 0.11 0 0
CUI: C1963899
Disease: Erosive gastroduodenitis
Erosive gastroduodenitis 		2 0 1 0.11 0 0
CUI: C2919706
Disease: Idiopathic rapidly progressive glomerulonephritis
Idiopathic rapidly progressive glomerulonephritis 		2 0 1 0.11 0 0
CUI: C3150926
Disease: Congenital dyserythropoietic anemia type IV
Congenital dyserythropoietic anemia type IV 		2 0 1 0.11 0 0
CUI: C4693796
Disease: RH-NULL, AMORPH TYPE
RH-NULL, AMORPH TYPE 		2 0 1 0.11 0 0
CUI: C0272052
Disease: Rh Deficiency Syndrome
Rh Deficiency Syndrome 		3 0 1 1.0E-01 0 0
CUI: C1565249
Disease: Mobility Limitation
Mobility Limitation 		3 0 1 1.0E-01 0 0
CUI: C1849387
Disease: Rh-Null, Regulator Type
Rh-Null, Regulator Type 		3 0 1 1.0E-01 0 0
CUI: C1859372
Disease: Calcification of Joints and Arteries
Calcification of Joints and Arteries 		3 0 1 1.0E-01 0 0
CUI: C2751719
Disease: ALCOHOL DEPENDENCE, PROTECTION AGAINST
ALCOHOL DEPENDENCE, PROTECTION AGAINST 		3 0 1 1.0E-01 0 0
CUI: C3281027
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7 		3 0 1 1.0E-01 0 0
CUI: C3887915
Disease: AERODIGESTIVE TRACT CANCER, SQUAMOUS CELL, ALCOHOL-RELATED, PROTECTION AGAINST
AERODIGESTIVE TRACT CANCER, SQUAMOUS CELL, ALCOHOL-RELATED, PROTECTION AGAINST 		3 0 1 1.0E-01 0 0
CUI: C4538570
Disease: COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY
COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY 		3 0 1 1.0E-01 0 0
CUI: C0014761
Disease: Erythroblastosis, Fetal
Erythroblastosis, Fetal 		16 1 2 9.1E-02 1 0.17
CUI: C1859495
Disease: Episodic hemolytic anemia
Episodic hemolytic anemia 		4 0 1 9.1E-02 0 0
CUI: C3888970
Disease: Embolic stroke of undetermined source
Embolic stroke of undetermined source 		4 0 1 9.1E-02 0 0
CUI: C0020497
Disease: Cortical Congenital Hyperostosis
Cortical Congenital Hyperostosis 		5 0 1 8.3E-02 0 0
CUI: C0344516
Disease: Coloboma of lens
Coloboma of lens 		5 0 1 8.3E-02 0 0
CUI: C0542141
Disease: Paralysis radial
Paralysis radial 		5 0 1 8.3E-02 0 0
CUI: C1306600
Disease: Radial nerve palsy
Radial nerve palsy 		5 0 1 8.3E-02 0 0
CUI: C1619634
Disease: erythrocyte sedimentation rate result
erythrocyte sedimentation rate result 		5 0 1 8.3E-02 0 0
CUI: C2676767
Disease: CD59 Deficiency
CD59 Deficiency 		5 0 1 8.3E-02 0 0
CUI: C4708599
Disease: Coloboma of choroid and retina
Coloboma of choroid and retina 		5 0 1 8.3E-02 0 0