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: C0002171
Disease: Alopecia Areata
Alopecia Areata 		0 54 0 0 1 1.9E-02
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis 		0 50 0 0 1 2.0E-02
CUI: C0018023
Disease: Nodular Goiter
Nodular Goiter 		0 12 0 0 1 8.3E-02
CUI: C0023896
Disease: Alcoholic Liver Diseases
Alcoholic Liver Diseases 		0 20 0 0 1 5.0E-02
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		0 26 0 0 1 3.8E-02
CUI: C0041408
Disease: Turner Syndrome
Turner Syndrome 		0 21 0 0 1 4.8E-02
CUI: C0042166
Disease: Uveitis, Intermediate
Uveitis, Intermediate 		0 10 0 0 1 1.0E-01
CUI: C0151468
Disease: Thyroid Gland Follicular Adenoma
Thyroid Gland Follicular Adenoma 		0 14 0 0 1 7.1E-02
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy 		0 116 0 0 1 8.6E-03
CUI: C0178468
Disease: Autoimmune thyroid disease
Autoimmune thyroid disease 		0 15 0 0 1 6.7E-02
CUI: C0206681
Disease: Adenocarcinoma, Clear Cell
Adenocarcinoma, Clear Cell 		0 6 0 0 1 0.17
CUI: C0206687
Disease: Carcinoma, Endometrioid
Carcinoma, Endometrioid 		0 12 0 0 1 8.3E-02
CUI: C0271815
Disease: Postpartum Thyroiditis
Postpartum Thyroiditis 		0 1 0 0 1 1.00
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia 		0 2 0 0 1 0.50
CUI: C1533172
Disease: Infantile nystagmus syndrome
Infantile nystagmus syndrome 		0 8 0 0 1 0.12
CUI: C1704321
Disease: Nephrotic Syndrome, Minimal Change
Nephrotic Syndrome, Minimal Change 		0 10 0 0 1 1.0E-01
CUI: C1704327
Disease: Bone Sarcoma
Bone Sarcoma 		0 4 0 0 1 0.25
CUI: C1845052
Disease: AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1 		0 4 0 0 1 0.25
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
SVEINSSON CHORIORETINAL ATROPHY 		0 30 0 0 1 3.3E-02
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome 		0 72 0 0 1 1.4E-02
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 1.4E-02 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 1 9.0E-04 0 0
CUI: C0000846
Disease: Agenesis
Agenesis 		161 0 1 5.9E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 5.0E-02 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		243 0 1 4.0E-03 0 0