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: C0001206
Disease: Acromegaly
Acromegaly 		138 0 1 6.4E-03 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		435 0 1 2.2E-03 0 0
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction 		50 0 1 1.4E-02 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related 		89 0 1 9.3E-03 0 0
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		282 0 1 3.3E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 1 1.8E-02 0 0
CUI: C0002726
Disease: Amyloidosis
Amyloidosis 		694 0 1 1.4E-03 0 0
CUI: C0002793
Disease: Anaplasia
Anaplasia 		538 0 1 1.8E-03 0 0
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		434 0 1 2.2E-03 0 0
CUI: C0003090
Disease: Ankylosis
Ankylosis 		15 0 1 2.9E-02 0 0
CUI: C0003126
Disease: Anosmia
Anosmia 		40 0 1 1.7E-02 0 0
CUI: C0003130
Disease: Anoxia
Anoxia 		287 0 1 3.3E-03 0 0
CUI: C0003486
Disease: Aortic Aneurysm
Aortic Aneurysm 		278 0 1 3.4E-03 0 0
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation 		88 0 1 9.3E-03 0 0
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		234 0 1 4.0E-03 0 0
CUI: C0003537
Disease: Aphasia
Aphasia 		86 0 1 9.5E-03 0 0
CUI: C0003614
Disease: Appendiceal Neoplasms
Appendiceal Neoplasms 		5 0 1 4.2E-02 0 0
CUI: C0003857
Disease: Congenital arteriovenous malformation
Congenital arteriovenous malformation 		163 0 1 5.5E-03 0 0
CUI: C0004059
Disease: aspirin intolerance
aspirin intolerance 		23 0 1 2.4E-02 0 0
CUI: C0004509
Disease: Azoospermia
Azoospermia 		254 0 1 3.7E-03 0 0
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		478 0 1 2.0E-03 0 0
CUI: C0004779
Disease: Basal Cell Nevus Syndrome
Basal Cell Nevus Syndrome 		74 0 1 1.1E-02 0 0
CUI: C0004936
Disease: Mental disorders
Mental disorders 		789 0 1 1.2E-03 0 0
CUI: C0004941
Disease: Behavioral Symptoms
Behavioral Symptoms 		45 0 1 1.6E-02 0 0
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		502 0 1 1.9E-03 0 0