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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		0 11 0 0 2 3.3E-02
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: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 2.0E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 2.0E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 2.0E-02
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait 		0 2 0 0 2 3.9E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 2 3.9E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 3.9E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 1.9E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 1.6E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 1 1.9E-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: 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 3.8E-02
CUI: C0003708
Disease: Arachnoiditis
Arachnoiditis 		1 0 1 5.3E-03 0 0
CUI: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 5.3E-03 0 0
CUI: C0005723
Disease: Oral paracoccidioidomycosis
Oral paracoccidioidomycosis 		1 0 1 5.3E-03 0 0
CUI: C0006915
Disease: Caplan Syndrome
Caplan Syndrome 		1 0 1 5.3E-03 0 0
CUI: C0007397
Disease: Catastrophic Illness
Catastrophic Illness 		1 0 1 5.3E-03 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 5.3E-03 0 0
CUI: C0009995
Disease: Cor Triatriatum
Cor Triatriatum 		1 0 1 5.3E-03 0 0