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 7.7E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 0.20
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		0 21 0 0 1 4.0E-02
CUI: C0282666
Disease: Very Low Birth Weight
Very Low Birth Weight 		0 2 0 0 1 0.17
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 0.25
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 7.9E-03
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome 		0 144 0 0 2 1.4E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 0.20
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 21 0 0 2 8.3E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 5.9E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 0.14
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 1 0.17
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 0.20
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 0.14
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 10 0 0 1 7.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 0.20
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 0.17
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 7.7E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 0.33
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 3.2E-02 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 3.2E-02 0 0
CUI: C0029307
Disease: Oroya Fever
Oroya Fever 		1 0 1 3.2E-02 0 0
CUI: C0040416
Disease: Tonic Pupil
Tonic Pupil 		1 0 1 3.2E-02 0 0
CUI: C0085222
Disease: Psoas Abscess
Psoas Abscess 		1 0 1 3.2E-02 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 3.2E-02 0 0