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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.0E-02
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		0 4 0 0 1 1.9E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 2.0E-02
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 2.0E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 4.0E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 2.0E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 2.0E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 2.0E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 1.7E-02
CUI: C3278384
Disease: HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY
HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY 		0 1 0 0 1 2.0E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.0E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.9E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.0E-02
CUI: C4014738
Disease: MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2 		0 4 0 0 1 1.9E-02
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 1.5E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.6E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 1.5E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory 		13 0 1 1.5E-03 0 0
CUI: C0001139
Disease: Acinetobacter Infections
Acinetobacter Infections 		1 0 1 1.6E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 1.5E-03 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 1.6E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.5E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis 		9 0 1 1.5E-03 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil 		2 0 1 1.6E-03 0 0
CUI: C0001576
Disease: Adnexal Diseases
Adnexal Diseases 		3 0 1 1.6E-03 0 0