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: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis 		1 0 1 6.2E-02 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 6.2E-02 0 0
CUI: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 6.2E-02 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 6.2E-02 0 0
CUI: C0274295
Disease: Brisket disease
Brisket disease 		1 0 1 6.2E-02 0 0
CUI: C0338822
Disease: Cycloid psychosis
Cycloid psychosis 		1 0 1 6.2E-02 0 0
CUI: C0344688
Disease: Patent Ductus Venosus
Patent Ductus Venosus 		1 0 1 6.2E-02 0 0
CUI: C0345183
Disease: Congenital constriction of pylorus
Congenital constriction of pylorus 		1 0 1 6.2E-02 0 0
CUI: C0432244
Disease: Osteodysplastic primordial dwarfism
Osteodysplastic primordial dwarfism 		1 0 1 6.2E-02 0 0
CUI: C0477597
Disease: Necrotising vasculopathy
Necrotising vasculopathy 		1 0 1 6.2E-02 0 0
CUI: C0521161
Disease: Vasculitic rash
Vasculitic rash 		1 0 1 6.2E-02 0 0
CUI: C0840564
Disease: Rupture of bladder
Rupture of bladder 		1 0 1 6.2E-02 0 0
CUI: C0858925
Disease: Deafness labyrinthine
Deafness labyrinthine 		1 0 1 6.2E-02 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery 		1 0 1 6.2E-02 0 0
CUI: C1332575
Disease: Bone Epithelioid Hemangioma
Bone Epithelioid Hemangioma 		1 0 1 6.2E-02 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF 		1 0 1 6.2E-02 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF 		1 0 1 6.2E-02 0 0
CUI: C1832253
Disease: INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF 		1 0 1 6.2E-02 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1 		1 0 1 6.2E-02 0 0
CUI: C1837187
Disease: MACULAR DEGENERATION, AGE-RELATED, 3
MACULAR DEGENERATION, AGE-RELATED, 3 		1 0 1 6.2E-02 0 0
CUI: C1859728
Disease: Coronary Sclerosis, Medial, of Infancy
Coronary Sclerosis, Medial, of Infancy 		1 0 1 6.2E-02 0 0
CUI: C1865267
Disease: Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly
Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly 		1 0 1 6.2E-02 0 0
CUI: C1867451
Disease: Pseudoxanthoma Elasticum, Heterozygous
Pseudoxanthoma Elasticum, Heterozygous 		1 0 1 6.2E-02 0 0
CUI: C1867453
Disease: Peau d'orange retinal changes
Peau d'orange retinal changes 		1 0 1 6.2E-02 0 0
CUI: C2033396
Disease: Yellow papule
Yellow papule 		1 0 1 6.2E-02 0 0