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: C0233689
Disease: Delusion of infidelity
Delusion of infidelity 		0 1 0 0 1 0.12
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 1 1.0E-01
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome 		0 1 0 0 1 0.12
CUI: C2677565
Disease: AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder) 		0 25 0 0 1 3.1E-02
CUI: C3148872
Disease: FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED 		0 3 0 0 1 1.0E-01
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute 		2 0 1 2.6E-03 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms 		13 0 1 2.5E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 2.5E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 2.5E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 2.4E-03 0 0
CUI: C0001197
Disease: Acrodermatitis
Acrodermatitis 		5 0 1 2.5E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 2.5E-03 0 0
CUI: C0001338
Disease: Herpetic Acute Necrotizing Encephalitis
Herpetic Acute Necrotizing Encephalitis 		5 0 1 2.5E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma 		9 0 1 2.5E-03 0 0
CUI: C0001511
Disease: Tissue Adhesions
Tissue Adhesions 		3 0 1 2.5E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 2.5E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 2.3E-03 0 0
CUI: C0001957
Disease: Alcohol Withdrawal Delirium
Alcohol Withdrawal Delirium 		23 0 1 2.4E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 2.5E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 2.1E-03 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 2.6E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 2.2E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 2.4E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia 		5 0 1 2.5E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder 		6 0 1 2.5E-03 0 0