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: C0276270
Disease: Oral papillomatosis
Oral papillomatosis 		1 0 1 7.0E-03 0 0
CUI: C0281952
Disease: Pseudohypothyroidism
Pseudohypothyroidism 		1 0 1 7.0E-03 0 0
CUI: C0282220
Disease: Amaurotic Familial Idiocy
Amaurotic Familial Idiocy 		1 0 1 7.0E-03 0 0
CUI: C0311386
Disease: Isosporiasis
Isosporiasis 		1 0 1 7.0E-03 0 0
CUI: C0332881
Disease: Congenital pseudoarthrosis
Congenital pseudoarthrosis 		1 0 1 7.0E-03 0 0
CUI: C0333372
Disease: Abscess cavity
Abscess cavity 		1 0 1 7.0E-03 0 0
CUI: C0334467
Disease: Fibrolipoma
Fibrolipoma 		1 0 1 7.0E-03 0 0
CUI: C0334689
Disease: C cell tumor
C cell tumor 		1 0 1 7.0E-03 0 0
CUI: C0340235
Disease: Bronchobiliary fistula
Bronchobiliary fistula 		1 0 1 7.0E-03 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 7.0E-03 0 0
CUI: C0349538
Disease: Malignant melanoma of anus
Malignant melanoma of anus 		1 0 1 7.0E-03 0 0
CUI: C0393725
Disease: Eating epilepsy
Eating epilepsy 		1 0 1 7.0E-03 0 0
CUI: C0399545
Disease: Anterior Diastema of Teeth
Anterior Diastema of Teeth 		1 0 1 7.0E-03 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 7.0E-03 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 7.0E-03 0 0
CUI: C0432360
Disease: Neurofibromatosis type 5
Neurofibromatosis type 5 		1 0 1 7.0E-03 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 7.0E-03 0 0
CUI: C0442774
Disease: Visual acuity, no light perception
Visual acuity, no light perception 		1 0 1 7.0E-03 0 0
CUI: C0455990
Disease: Immune Hydrops Fetalis
Immune Hydrops Fetalis 		1 0 1 7.0E-03 0 0
CUI: C0456086
Disease: Intrapartum fetal hypoxia
Intrapartum fetal hypoxia 		1 0 1 7.0E-03 0 0
CUI: C0519055
Disease: Renal involvement in scleroderma
Renal involvement in scleroderma 		1 0 1 7.0E-03 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 7.0E-03 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 7.0E-03 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 7.0E-03 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 7.0E-03 0 0