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: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 2 1 0.25 1 6.7E-02
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 0.25 0 0
CUI: C0424939
Disease: Learning difficulties
Learning difficulties 		6 0 2 0.25 0 0
CUI: C0549608
Disease: VEINS/LYMPHATICS
VEINS/LYMPHATICS 		1 0 1 0.25 0 0
CUI: C0796046
Disease: Gurrieri Sammito Bellussi syndrome
Gurrieri Sammito Bellussi syndrome 		1 0 1 0.25 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 0.25 0 0
CUI: C1306574
Disease: Botryoid rhabdomyosarcoma
Botryoid rhabdomyosarcoma 		1 0 1 0.25 0 0
CUI: C1332899
Disease: Cerebellar Glioblastoma
Cerebellar Glioblastoma 		6 0 2 0.25 0 0
CUI: C1333081
Disease: Colloid Carcinoma of the Pancreas
Colloid Carcinoma of the Pancreas 		1 0 1 0.25 0 0
CUI: C1333308
Disease: Distal Bile Duct Carcinoma
Distal Bile Duct Carcinoma 		1 0 1 0.25 0 0
CUI: C1704453
Disease: Oncocytic Schneiderian papilloma
Oncocytic Schneiderian papilloma 		1 0 1 0.25 0 0
CUI: C1835465
Disease: Short stature, postnatal
Short stature, postnatal 		1 0 1 0.25 0 0
CUI: C1838329
Disease: APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS 		1 0 1 0.25 0 0
CUI: C1839125
Disease: Say Meyer syndrome
Say Meyer syndrome 		1 0 1 0.25 0 0
CUI: C1839727
Disease: Mental Retardation with Spastic Paraplegia
Mental Retardation with Spastic Paraplegia 		1 0 1 0.25 0 0
CUI: C1842881
Disease: Dilated aortic root
Dilated aortic root 		1 0 1 0.25 0 0
CUI: C1856911
Disease: Ivory epiphyses
Ivory epiphyses 		1 0 1 0.25 0 0
CUI: C1859478
Disease: Hypoplasia of proximal fibula
Hypoplasia of proximal fibula 		1 0 1 0.25 0 0
CUI: C2678046
Disease: Mental Retardation, X-Linked, Syndromic, Turner Type
Mental Retardation, X-Linked, Syndromic, Turner Type 		1 0 1 0.25 0 0
CUI: C2721606
Disease: Bladder dysplasia
Bladder dysplasia 		1 0 1 0.25 0 0
CUI: C2873755
Disease: Triple gene defect alpha thalassemia
Triple gene defect alpha thalassemia 		1 0 1 0.25 0 0
CUI: C3161173
Disease: Hemoglobin H Constant Spring
Hemoglobin H Constant Spring 		1 0 1 0.25 0 0
CUI: C3161175
Disease: Hydrops fetalis due to alpha thalassemia
Hydrops fetalis due to alpha thalassemia 		1 0 1 0.25 0 0
CUI: C3281203
Disease: CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL
CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL 		1 0 1 0.25 0 0
CUI: C3809005
Disease: CARDIOFACIOCUTANEOUS SYNDROME 2
CARDIOFACIOCUTANEOUS SYNDROME 2 		1 0 1 0.25 0 0