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: C0848034
Disease: Low IQ
Low IQ 		4 0 2 0.33 0 0
CUI: C0035468
Disease: Rhinoscleroma
Rhinoscleroma 		1 0 1 0.25 0 0
CUI: C0267642
Disease: Childhood celiac disease
Childhood celiac disease 		1 0 1 0.25 0 0
CUI: C0751740
Disease: Lenticulostriate Vasculopathy
Lenticulostriate Vasculopathy 		1 0 1 0.25 0 0
CUI: C1332355
Disease: Autoimmune Hepatitis with Centrilobular Necrosis
Autoimmune Hepatitis with Centrilobular Necrosis 		6 3 2 0.25 1 0.14
CUI: C1969286
Disease: Hypoplastic distal radial epiphyses
Hypoplastic distal radial epiphyses 		1 0 1 0.25 0 0
CUI: C1969287
Disease: Expanded phalanges with widened medullary cavities
Expanded phalanges with widened medullary cavities 		1 0 1 0.25 0 0
CUI: C1969288
Disease: Expanded metacarpals with widened medullary cavities
Expanded metacarpals with widened medullary cavities 		1 0 1 0.25 0 0
CUI: C1969289
Disease: Expanded metatarsals with widened medullary cavities
Expanded metatarsals with widened medullary cavities 		1 0 1 0.25 0 0
CUI: C1969291
Disease: Aortic arch calcification
Aortic arch calcification 		1 0 1 0.25 0 0
CUI: C2827448
Disease: Childhood Diabetes Mellitus
Childhood Diabetes Mellitus 		1 0 1 0.25 0 0
CUI: C2936833
Disease: Mycobacterium tuberculosis, susceptibility to infection by
Mycobacterium tuberculosis, susceptibility to infection by 		1 0 1 0.25 0 0
CUI: C4025055
Disease: Hypoplasia of the tooth germ
Hypoplasia of the tooth germ 		1 0 1 0.25 0 0
CUI: C0025062
Disease: Mediastinal Emphysema
Mediastinal Emphysema 		2 0 1 0.20 0 0
CUI: C0235956
Disease: Absence attacks
Absence attacks 		2 0 1 0.20 0 0
CUI: C0751622
Disease: Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related
Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related 		2 0 1 0.20 0 0
CUI: C0935560
Disease: Multiple disability
Multiple disability 		2 1 1 0.20 1 0.20
CUI: C3888244
Disease: AICARDI-GOUTIERES SYNDROME 7
AICARDI-GOUTIERES SYNDROME 7 		2 0 1 0.20 0 0
CUI: C4225427
Disease: SINGLETON-MERTEN SYNDROME 1
SINGLETON-MERTEN SYNDROME 1 		2 0 1 0.20 0 0
CUI: C0152084
Disease: Jaccoud's syndrome
Jaccoud's syndrome 		3 0 1 0.17 0 0
CUI: C0206744
Disease: T-Lymphocytopenia, Idiopathic CD4-Positive
T-Lymphocytopenia, Idiopathic CD4-Positive 		3 0 1 0.17 0 0
CUI: C0342553
Disease: Juvenile Graves' disease
Juvenile Graves' disease 		3 0 1 0.17 0 0
CUI: C1280469
Disease: Podoconiosis
Podoconiosis 		3 0 1 0.17 0 0
CUI: C1535942
Disease: Polyglandular Type III Autoimmune Syndrome
Polyglandular Type III Autoimmune Syndrome 		10 0 2 0.17 0 0
CUI: C0031887
Disease: Picornaviridae Infections
Picornaviridae Infections 		4 0 1 0.14 0 0