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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.3E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 1.2E-02
CUI: C2930980
Disease: Malignant hyperthermia susceptibility type 1
Malignant hyperthermia susceptibility type 1 		0 97 0 0 1 5.7E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.3E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.3E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 1.2E-02
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 2.7E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 2.7E-03 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis 		4 0 1 2.7E-03 0 0
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction 		24 0 1 2.6E-03 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma 		21 0 1 2.6E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma 		9 0 1 2.7E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 2.7E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 0 1 2.7E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases 		9 2 1 2.7E-03 1 1.2E-02
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms 		23 0 1 2.6E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 2.5E-03 0 0
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		45 0 1 2.4E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 2.4E-03 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease 		2 0 1 2.7E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 2.6E-03 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis 		13 0 1 2.6E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 2.6E-03 0 0
CUI: C0002690
Disease: Amputation Stumps
Amputation Stumps 		11 0 1 2.7E-03 0 0
CUI: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia 		24 0 1 2.6E-03 0 0