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: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy 		23 0 8 0.17 0 0
CUI: C1851720
Disease: Adrenocortical cytomegaly
Adrenocortical cytomegaly 		6 0 4 0.12 0 0
CUI: C1851722
Disease: Overgrowth of external genitalia
Overgrowth of external genitalia 		6 0 4 0.12 0 0
CUI: C1851733
Disease: Pancreatic hyperplasia
Pancreatic hyperplasia 		6 0 4 0.12 0 0
CUI: C4021539
Disease: Posterior helix pit
Posterior helix pit 		9 0 4 0.11 0 0
CUI: C1335299
Disease: Pancreatic Adenosquamous Carcinoma
Pancreatic Adenosquamous Carcinoma 		13 0 4 1.0E-01 0 0
CUI: C0022739
Disease: Klippel-Trenaunay-Weber Syndrome
Klippel-Trenaunay-Weber Syndrome 		14 0 4 9.8E-02 0 0
CUI: C1969144
Disease: Renal cortical cysts
Renal cortical cysts 		14 0 4 9.8E-02 0 0
CUI: C0542518
Disease: Enlarged kidney
Enlarged kidney 		27 0 5 9.4E-02 0 0
CUI: C1367536
Disease: Nasopharyngeal Angiofibroma
Nasopharyngeal Angiofibroma 		17 0 4 9.1E-02 0 0
CUI: C4317089
Disease: Infantile hemangioma
Infantile hemangioma 		82 0 9 8.7E-02 0 0
CUI: C0796160
Disease: MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE
MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE 		32 0 5 8.6E-02 0 0
CUI: C0750887
Disease: Adrenal Cancer
Adrenal Cancer 		20 0 4 8.5E-02 0 0
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain 		46 0 6 8.5E-02 0 0
CUI: C0221766
Disease: Diastasis recti
Diastasis recti 		22 0 4 8.2E-02 0 0
CUI: C0010276
Disease: Craniopharyngioma
Craniopharyngioma 		64 0 7 8.0E-02 0 0
CUI: C0278652
Disease: Childhood Craniopharyngioma
Childhood Craniopharyngioma 		38 0 5 7.8E-02 0 0
CUI: C0278875
Disease: Adult Craniopharyngioma
Adult Craniopharyngioma 		38 0 5 7.8E-02 0 0
CUI: C3267003
Disease: Vascular endothelial growth factor overexpression
Vascular endothelial growth factor overexpression 		26 0 4 7.5E-02 0 0
CUI: C0206733
Disease: Strawberry nevus of skin
Strawberry nevus of skin 		112 0 10 7.5E-02 0 0
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		55 0 6 7.5E-02 0 0
CUI: C0861876
Disease: Recurrent Hepatocellular Carcinoma
Recurrent Hepatocellular Carcinoma 		12 0 3 7.5E-02 0 0
CUI: C1858033
Disease: Asymmetry of the thorax
Asymmetry of the thorax 		12 0 3 7.5E-02 0 0
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases 		13 0 3 7.3E-02 0 0
CUI: C0338596
Disease: Spastic cerebral palsy
Spastic cerebral palsy 		13 0 3 7.3E-02 0 0