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: C0004093
Disease: Asthenia
Asthenia 		0 3 0 0 1 2.6E-02
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		0 12 0 0 1 2.1E-02
CUI: C0020875
Disease: Ileal Diseases
Ileal Diseases 		0 7 0 0 1 2.3E-02
CUI: C0237967
Disease: pediatric AIDS
pediatric AIDS 		0 2 0 0 1 2.6E-02
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 2.7E-02
CUI: C0334070
Disease: Maturation defect
Maturation defect 		0 2 0 0 1 2.6E-02
CUI: C0376670
Disease: Pancreatitis, Alcoholic
Pancreatitis, Alcoholic 		0 86 0 0 1 8.2E-03
CUI: C0406191
Disease: Pseudofolliculitis
Pseudofolliculitis 		0 1 0 0 1 2.7E-02
CUI: C0543697
Disease: Mixed cryoglobulinemia
Mixed cryoglobulinemia 		0 5 0 0 1 2.4E-02
CUI: C0549410
Disease: Palmar-plantar erythrodysesthesia syndrome
Palmar-plantar erythrodysesthesia syndrome 		0 8 0 0 1 2.3E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 2.7E-02
CUI: C0746883
Disease: Febrile Neutropenia
Febrile Neutropenia 		0 14 0 0 1 2.0E-02
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		0 10 0 0 1 2.2E-02
CUI: C0852711
Disease: Sickle Cell Dactylitis
Sickle Cell Dactylitis 		0 7 0 0 1 2.3E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 2.2E-02
CUI: C1504532
Disease: Post transplant diabetes mellitus
Post transplant diabetes mellitus 		0 11 0 0 1 2.1E-02
CUI: C1533172
Disease: Infantile nystagmus syndrome
Infantile nystagmus syndrome 		0 8 0 0 2 4.7E-02
CUI: C1568868
Disease: Oral Mucositis
Oral Mucositis 		0 16 0 0 1 1.9E-02
CUI: C1698259
Disease: HCV coinfection
HCV coinfection 		0 5 0 0 1 2.4E-02
CUI: C1861502
Disease: COLCHICINE RESISTANCE
COLCHICINE RESISTANCE 		0 3 0 0 1 2.6E-02
CUI: C2750509
Disease: Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 		0 4 0 0 1 2.5E-02
CUI: C3203671
Disease: CYP2D6 polymorphism
CYP2D6 polymorphism 		0 5 0 0 1 2.4E-02
CUI: C3826394
Disease: Epilepsy in children
Epilepsy in children 		0 1 0 0 1 2.7E-02
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 3.8E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 5.6E-03 0 0