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: C0009398
Disease: Color vision defect
Color vision defect 		0 4 0 0 1 2.8E-02
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood 		0 20 0 0 1 1.9E-02
CUI: C0239377
Disease: Arm Pain
Arm Pain 		0 6 0 0 1 2.6E-02
CUI: C0278139
Disease: Moderate pain
Moderate pain 		0 1 0 0 1 3.0E-02
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 3.0E-02
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 2.9E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon 		0 1 0 0 1 3.0E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 2.4E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 3.0E-02
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia 		0 4 0 0 1 2.8E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.0E-02
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 1.2E-02 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.3E-02 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 9.8E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 1.1E-02 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 1.3E-02 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.2E-02 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma 		8 0 1 1.2E-02 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma 		9 0 1 1.2E-02 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 4 1 1.2E-02 1 2.8E-02
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 1 6.2E-03 0 0
CUI: C0001818
Disease: Agoraphobia
Agoraphobia 		29 0 1 9.7E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		13 0 1 1.1E-02 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia 		5 0 1 1.3E-02 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity 		2 0 1 1.3E-02 0 0