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 1.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.4E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.3E-02
CUI: C0279084
Disease: Kaposi's sarcoma classical type
Kaposi's sarcoma classical type 		0 3 0 0 1 1.4E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 2.7E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 5.2E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.4E-02
CUI: C1135196
Disease: Heart Failure, Diastolic
Heart Failure, Diastolic 		0 9 0 0 1 1.3E-02
CUI: C1290073
Disease: Acute mucositis
Acute mucositis 		0 1 0 0 1 1.4E-02
CUI: C3150344
Disease: HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED
HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED 		0 24 0 0 1 1.1E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 1.4E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 1 1.4E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.4E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.4E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 10 0 0 1 1.3E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.4E-02
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0 355 0 0 1 2.4E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 2.8E-02
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 3.9E-03 0 0
CUI: C0002897
Disease: Anemia, Splenic
Anemia, Splenic 		1 0 1 3.9E-03 0 0
CUI: C0003756
Disease: Arenaviridae Infections
Arenaviridae Infections 		1 0 1 3.9E-03 0 0
CUI: C0005723
Disease: Oral paracoccidioidomycosis
Oral paracoccidioidomycosis 		1 0 1 3.9E-03 0 0
CUI: C0005911
Disease: Body Weight Changes
Body Weight Changes 		1 0 1 3.9E-03 0 0
CUI: C0007397
Disease: Catastrophic Illness
Catastrophic Illness 		1 0 1 3.9E-03 0 0
CUI: C0009792
Disease: Consciousness Disorders
Consciousness Disorders 		1 0 1 3.9E-03 0 0