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: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 4.8E-02
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 9.5E-02
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 1 4.3E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 4.8E-02
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 4.5E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 4.8E-02
CUI: C1836482
Disease: Li-Fraumeni Syndrome 2
Li-Fraumeni Syndrome 2 		0 11 0 0 1 3.2E-02
CUI: C1840084
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, SLOW PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, SLOW PROGRESSION TO 		0 1 0 0 1 4.8E-02
CUI: C1858433
Disease: BREAST AND COLORECTAL CANCER, SUSCEPTIBILITY TO
BREAST AND COLORECTAL CANCER, SUSCEPTIBILITY TO 		0 7 0 0 1 3.7E-02
CUI: C1858439
Disease: CANCER OF MULTIPLE TYPES, SUSCEPTIBILITY TO
CANCER OF MULTIPLE TYPES, SUSCEPTIBILITY TO 		0 1 0 0 1 4.8E-02
CUI: C3469524
Disease: PROSTATE CANCER, SUSCEPTIBILITY TO
PROSTATE CANCER, SUSCEPTIBILITY TO 		0 6 0 0 1 3.8E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 4.8E-02
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis 		4 0 1 1.5E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 1.5E-03 0 0
CUI: C0001249
Disease: Actinobacillus Infections
Actinobacillus Infections 		1 0 1 1.5E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.5E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 1.5E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 1.5E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 4 1 1.5E-03 2 8.7E-02
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 1.5E-03 0 0
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism 		1 0 1 1.5E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 1.4E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 1.5E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 1.5E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 1.5E-03 0 0