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: C1319016
Disease: Nephrogenic rest, intralobar
Nephrogenic rest, intralobar 		1 0 1 1.00 0 0
CUI: C1860268
Disease: Gonadal tissue inappropriate for external genitalia or chromosomal sex
Gonadal tissue inappropriate for external genitalia or chromosomal sex 		1 0 1 1.00 0 0
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		1 9 1 1.00 2 0.20
CUI: C4024632
Disease: Gonadal dysgenesis with female appearance, male
Gonadal dysgenesis with female appearance, male 		2 0 1 0.50 0 0
CUI: C4703595
Disease: Increased proinsulin:insulin ratio
Increased proinsulin:insulin ratio 		2 0 1 0.50 0 0
CUI: C2931803
Disease: Deletion 11p13
Deletion 11p13 		3 0 1 0.33 0 0
CUI: C0023439
Disease: Leukemia, Eosinophilic, Acute
Leukemia, Eosinophilic, Acute 		4 0 1 0.25 0 0
CUI: C0344542
Disease: Aniridia type 1
Aniridia type 1 		4 87 1 0.25 1 1.1E-02
CUI: C1333003
Disease: Childhood Kidney Neoplasm
Childhood Kidney Neoplasm 		4 0 1 0.25 0 0
CUI: C1832671
Disease: Dysfunction of lateral corticospinal tracts
Dysfunction of lateral corticospinal tracts 		4 0 1 0.25 0 0
CUI: C0751374
Disease: Schwannomatosis, Plexiform
Schwannomatosis, Plexiform 		5 0 1 0.20 0 0
CUI: C1335976
Disease: Skull Base Meningioma
Skull Base Meningioma 		5 0 1 0.20 0 0
CUI: C0006288
Disease: Bronchopulmonary Sequestration
Bronchopulmonary Sequestration 		6 0 1 0.17 0 0
CUI: C0242404
Disease: Myofibroblastoma
Myofibroblastoma 		6 0 1 0.17 0 0
CUI: C0950122
Disease: Frasier Syndrome
Frasier Syndrome 		6 17 1 0.17 2 0.11
CUI: C1333468
Disease: Esophageal Squamous Intraepithelial Neoplasia
Esophageal Squamous Intraepithelial Neoplasia 		6 0 1 0.17 0 0
CUI: C1864445
Disease: Histiocytosis with joint contractures and sensorineural deafness
Histiocytosis with joint contractures and sensorineural deafness 		6 0 1 0.17 0 0
CUI: C3494522
Disease: Hypergonadotropic Ovarian Failure, X-Linked
Hypergonadotropic Ovarian Failure, X-Linked 		6 0 1 0.17 0 0
CUI: C0269209
Disease: Hydrometrocolpos
Hydrometrocolpos 		7 0 1 0.14 0 0
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 7 1 0.14 1 0.11
CUI: C1840452
Disease: Hyaloideoretinal degeneration of Wagner
Hyaloideoretinal degeneration of Wagner 		7 0 1 0.14 0 0
CUI: C2861580
Disease: Chronic myeloid leukemia, BCR/ABL-positive
Chronic myeloid leukemia, BCR/ABL-positive 		7 0 1 0.14 0 0
CUI: C4551835
Disease: Intralobar nephroblastomatosis
Intralobar nephroblastomatosis 		7 0 1 0.14 0 0
CUI: C4552079
Disease: Premature Ovarian Failure 1
Premature Ovarian Failure 1 		7 0 1 0.14 0 0
CUI: C0036769
Disease: Sertoli Cell Tumor
Sertoli Cell Tumor 		9 0 1 0.11 0 0