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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.7E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.0E-02
CUI: C0154038
Disease: Benign neoplasm of thyroid gland
Benign neoplasm of thyroid gland 		0 4 0 0 1 1.9E-02
CUI: C0346398
Disease: Mixed follicular and papillary thyroid carcinoma
Mixed follicular and papillary thyroid carcinoma 		0 8 0 0 1 1.8E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 2.0E-02
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases 		0 1 0 0 1 2.0E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 1.6E-02
CUI: C1444844
Disease: Juvenile idiopathic arthritis, enthesitis related arthritis
Juvenile idiopathic arthritis, enthesitis related arthritis 		0 1 0 0 1 2.0E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 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: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 10 0 0 1 1.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.0E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 2.0E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 1.7E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 3.9E-02
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 9.8E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.0E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 7.3E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 1 3.3E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 9.0E-03 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis 		11 0 1 9.8E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis 		9 0 1 1.0E-02 0 0
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction 		24 0 1 8.7E-03 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma 		21 0 1 8.9E-03 0 0