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: C0267356
Disease: Duodenal perforation
Duodenal perforation 		2 0 2 0.40 0 0
CUI: C1832229
Disease: Rieger syndrome 2 (disorder)
Rieger syndrome 2 (disorder) 		2 0 2 0.40 0 0
CUI: C2875014
Disease: Acute disseminated encephalitis and encephalomyelitis (ADEM)
Acute disseminated encephalitis and encephalomyelitis (ADEM) 		3 0 2 0.33 0 0
CUI: C0393602
Disease: Isolated cervical dystonia
Isolated cervical dystonia 		1 0 1 0.20 0 0
CUI: C0730364
Disease: Idiopathic polypoidal choroidal vasculopathy
Idiopathic polypoidal choroidal vasculopathy 		1 0 1 0.20 0 0
CUI: C1843542
Disease: T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC
T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC 		1 0 1 0.20 0 0
CUI: C1859624
Disease: Defective B cell differentiation
Defective B cell differentiation 		1 0 1 0.20 0 0
CUI: C2931837
Disease: Familial hypertryptophanemia
Familial hypertryptophanemia 		1 0 1 0.20 0 0
CUI: C3825373
Disease: Hodgkin's disease in children
Hodgkin's disease in children 		1 0 1 0.20 0 0
CUI: C0340305
Disease: Inferior Wall Myocardial Infarction
Inferior Wall Myocardial Infarction 		2 0 1 0.17 0 0
CUI: C1876175
Disease: Ataxia-Telangiectasia Variant
Ataxia-Telangiectasia Variant 		2 0 1 0.17 0 0
CUI: C4017102
Disease: ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY
ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY 		2 0 1 0.17 0 0
CUI: C0263606
Disease: Early radiation dermatitis
Early radiation dermatitis 		3 0 1 0.14 0 0
CUI: C0862636
Disease: Adenocarcinoma of the prostate metastatic
Adenocarcinoma of the prostate metastatic 		11 0 2 0.14 0 0
CUI: C3249875
Disease: Laryngopharyngeal Cancer
Laryngopharyngeal Cancer 		3 0 1 0.14 0 0
CUI: C3547187
Disease: response to metformin
response to metformin 		3 0 1 0.14 0 0
CUI: C0701818
Disease: Choledocholithiasis
Choledocholithiasis 		12 0 2 0.13 0 0
CUI: C4024276
Disease: Peripheral Schwannoma
Peripheral Schwannoma 		4 0 1 0.12 0 0
CUI: C0410173
Disease: Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder) 		14 0 2 0.12 0 0
CUI: C0339808
Disease: House dust mite allergy
House dust mite allergy 		5 0 1 0.11 0 0
CUI: C0520933
Disease: Abnormal spermatogenesis
Abnormal spermatogenesis 		5 0 1 0.11 0 0
CUI: C0524610
Disease: Chronic Alcoholic Hepatitis
Chronic Alcoholic Hepatitis 		5 0 1 0.11 0 0
CUI: C0555202
Disease: Malignant lymphoma - lymphocytic, intermediate differentiation
Malignant lymphoma - lymphocytic, intermediate differentiation 		5 0 1 0.11 0 0
CUI: C0029440
Disease: Osteoma
Osteoma 		6 0 1 1.0E-01 0 0
CUI: C3160891
Disease: Hormone-dependent prostate cancer
Hormone-dependent prostate cancer 		6 0 1 1.0E-01 0 0