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 5.6E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.0E-01
CUI: C0085932
Disease: Bullous Dermatitis
Bullous Dermatitis 		0 1 0 0 1 1.0E-01
CUI: C0271815
Disease: Postpartum Thyroiditis
Postpartum Thyroiditis 		0 1 0 0 1 1.0E-01
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.0E-01
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 7.6E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 1.0E-01
CUI: C1275047
Disease: Radiation-induced xerostomia
Radiation-induced xerostomia 		0 1 0 0 1 1.0E-01
CUI: C1845052
Disease: AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1 		0 4 0 0 1 7.7E-02
CUI: C1876181
Disease: EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS
EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS 		0 2 0 0 1 9.1E-02
CUI: C3203671
Disease: CYP2D6 polymorphism
CYP2D6 polymorphism 		0 5 0 0 1 7.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.0E-01
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.0E-01
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		0 4 0 0 1 7.7E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 9.1E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 5.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 8.3E-02
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 6.7E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.0E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis 		161 0 1 4.1E-03 0 0
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis 		22 0 1 9.4E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.1E-02 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 7.4E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory 		13 0 1 1.0E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 9.6E-03 0 0