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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 2.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.8E-02
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 3 4.7E-02
CUI: C2930987
Disease: Paranasal sinus teratocarcinosarcoma (type)
Paranasal sinus teratocarcinosarcoma (type) 		0 1 0 0 1 2.8E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.8E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.8E-02
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 2.9E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 2.9E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 2.9E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory 		13 0 1 2.9E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 2.9E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 2.9E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 3.0E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 2.9E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis 		9 0 1 2.9E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 2.9E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 2.9E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 2.9E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases 		9 0 1 2.9E-03 0 0
CUI: C0001828
Disease: Agricultural Workers' Diseases
Agricultural Workers' Diseases 		1 0 1 3.0E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 2.9E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 2.9E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 2.5E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia 		5 0 1 2.9E-03 0 0
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		14 0 1 2.8E-03 0 0