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: C1860048
Disease: Temporal bossing
Temporal bossing 		2 0 1 0.11 0 0
CUI: C1861226
Disease: Small abnormally formed scapulae
Small abnormally formed scapulae 		2 0 1 0.11 0 0
CUI: C1867487
Disease: Childhood onset short-limb short stature
Childhood onset short-limb short stature 		2 0 1 0.11 0 0
CUI: C1883722
Disease: Stage 0a Bladder Urothelial Carcinoma AJCC v6 and v7
Stage 0a Bladder Urothelial Carcinoma AJCC v6 and v7 		2 0 1 0.11 0 0
CUI: C2014414
Disease: orthopedic disorders
orthopedic disorders 		2 0 1 0.11 0 0
CUI: C4025679
Disease: Stippled chondral calcification
Stippled chondral calcification 		2 0 1 0.11 0 0
CUI: C0235754
Disease: Bladder papilloma
Bladder papilloma 		3 0 1 1.0E-01 0 0
CUI: C0302319
Disease: Porokeratosis, Linear
Porokeratosis, Linear 		3 0 1 1.0E-01 0 0
CUI: C0333184
Disease: Calcific stenosis
Calcific stenosis 		3 0 1 1.0E-01 0 0
CUI: C0392439
Disease: Acrodermatitis continua of Hallopeau
Acrodermatitis continua of Hallopeau 		3 0 1 1.0E-01 0 0
CUI: C0522618
Disease: Focal dysplasia
Focal dysplasia 		3 0 1 1.0E-01 0 0
CUI: C0741032
Disease: Refractory angina
Refractory angina 		3 0 1 1.0E-01 0 0
CUI: C1849993
Disease: Calcific stippling
Calcific stippling 		3 0 1 1.0E-01 0 0
CUI: C1859235
Disease: Intrahepatic biliary dysgenesis
Intrahepatic biliary dysgenesis 		3 0 1 1.0E-01 0 0
CUI: C1861217
Disease: Small foramen magnum
Small foramen magnum 		3 0 1 1.0E-01 0 0
CUI: C1863200
Disease: Lacrimal gland hypoplasia
Lacrimal gland hypoplasia 		3 0 1 1.0E-01 0 0
CUI: C1864436
Disease: Muenke Syndrome
Muenke Syndrome 		3 0 1 1.0E-01 0 0
CUI: C1867981
Disease: POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1
POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1 		3 0 1 1.0E-01 0 0
CUI: C1959626
Disease: Mevalonic Aciduria
Mevalonic Aciduria 		3 0 1 1.0E-01 0 0
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
Plasminogen Deficiency, Type I 		3 0 1 1.0E-01 0 0
CUI: C2674173
Disease: Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans 		3 0 1 1.0E-01 0 0
CUI: C3278024
Disease: Enlarged cerebellum
Enlarged cerebellum 		3 0 1 1.0E-01 0 0
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke 		3 0 1 1.0E-01 0 0
CUI: C4015344
Disease: PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER
PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER 		3 0 1 1.0E-01 0 0
CUI: C4021377
Disease: Prominent crus of helix
Prominent crus of helix 		3 0 1 1.0E-01 0 0