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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		0 4 0 0 1 2.9E-03
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		0 11 0 0 1 2.8E-03
CUI: C0085293
Disease: Hepatitis E
Hepatitis E 		0 2 0 0 1 2.9E-03
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis 		0 31 0 0 1 2.7E-03
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 2.9E-03
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		0 8 0 0 1 2.8E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 2.9E-03
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy 		0 120 0 0 1 2.2E-03
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		0 3 0 0 1 2.9E-03
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait 		0 2 0 0 1 2.9E-03
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 1 2.9E-03
CUI: C0854135
Disease: Pseudomonas aeruginosa infection
Pseudomonas aeruginosa infection 		0 1 0 0 1 2.9E-03
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 2.9E-03
CUI: C1264195
Disease: Refractory anemia with ringed sideroblasts
Refractory anemia with ringed sideroblasts 		0 3 0 0 1 2.9E-03
CUI: C0007761
Disease: Myoclonic Cerebellar Dyssynergia
Myoclonic Cerebellar Dyssynergia 		1 0 1 6.8E-03 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 6.8E-03 0 0
CUI: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic 		1 0 1 6.8E-03 0 0
CUI: C0016724
Disease: Froehlich's Syndrome
Froehlich's Syndrome 		1 0 1 6.8E-03 0 0
CUI: C0017409
Disease: Herpes Zoster Oticus
Herpes Zoster Oticus 		1 0 1 6.8E-03 0 0
CUI: C0037768
Disease: Spasmophilia
Spasmophilia 		1 0 1 6.8E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 6.8E-03 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 6.8E-03 0 0
CUI: C0178272
Disease: Disorder of pulmonary circulation
Disorder of pulmonary circulation 		1 0 1 6.8E-03 0 0
CUI: C0235462
Disease: Anginal attack
Anginal attack 		1 0 1 6.8E-03 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 6.8E-03 0 0