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: C0423319
Disease: Atrophic iris
Atrophic iris 		9 0 1 6.7E-02 0 0
CUI: C0741237
Disease: arthritis symptoms
arthritis symptoms 		9 0 1 6.7E-02 0 0
CUI: C2700265
Disease: Waardenburg Syndrome Type 2
Waardenburg Syndrome Type 2 		9 0 1 6.7E-02 0 0
CUI: C0042111
Disease: Urticaria Pigmentosa
Urticaria Pigmentosa 		10 0 1 6.2E-02 0 0
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		10 0 1 6.2E-02 0 0
CUI: C0242490
Disease: Enthesopathy
Enthesopathy 		11 0 1 5.9E-02 0 0
CUI: C2986691
Disease: Inherited bone marrow failure syndrome
Inherited bone marrow failure syndrome 		11 0 1 5.9E-02 0 0
CUI: C0022738
Disease: Klippel-Feil Syndrome
Klippel-Feil Syndrome 		12 0 1 5.6E-02 0 0
CUI: C0344312
Disease: White forelock
White forelock 		12 0 1 5.6E-02 0 0
CUI: C1536075
Disease: Sudden unexplained death in epilepsy
Sudden unexplained death in epilepsy 		12 0 1 5.6E-02 0 0
CUI: C2676137
Disease: Diamond-Blackfan Anemia 1
Diamond-Blackfan Anemia 1 		12 0 1 5.6E-02 0 0
CUI: C4082168
Disease: Partial duplication of thumb phalanx
Partial duplication of thumb phalanx 		12 0 1 5.6E-02 0 0
CUI: C4726609
Disease: Resectable Pancreatic Ductal Adenocarcinoma
Resectable Pancreatic Ductal Adenocarcinoma 		12 0 1 5.6E-02 0 0
CUI: C0002982
Disease: Angioid Streaks
Angioid Streaks 		13 0 1 5.3E-02 0 0
CUI: C0040149
Disease: Subacute thyroiditis
Subacute thyroiditis 		13 0 1 5.3E-02 0 0
CUI: C0085662
Disease: Macrocytosis
Macrocytosis 		13 0 1 5.3E-02 0 0
CUI: C0154823
Disease: Retinal defect
Retinal defect 		13 0 1 5.3E-02 0 0
CUI: C0178540
Disease: Cerebral Hypoxia-Ischemia
Cerebral Hypoxia-Ischemia 		13 0 1 5.3E-02 0 0
CUI: C0522624
Disease: Subcutaneous panniculitis-like T-cell lymphoma
Subcutaneous panniculitis-like T-cell lymphoma 		13 0 1 5.3E-02 0 0
CUI: C0858681
Disease: Vitiligo vulgaris
Vitiligo vulgaris 		13 0 1 5.3E-02 0 0
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines 		13 0 1 5.3E-02 0 0
CUI: C4285959
Disease: Erosive arthritis
Erosive arthritis 		13 0 1 5.3E-02 0 0
CUI: C0271980
Disease: beta^0^ Thalassemia
beta^0^ Thalassemia 		34 0 2 5.1E-02 0 0
CUI: C0009681
Disease: Anomalous pulmonary artery
Anomalous pulmonary artery 		14 0 1 5.0E-02 0 0
CUI: C0151491
Disease: Congenital musculoskeletal anomalies
Congenital musculoskeletal anomalies 		14 0 1 5.0E-02 0 0