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: C4225321
Disease: ZIMMERMANN-LABAND SYNDROME 2
ZIMMERMANN-LABAND SYNDROME 2 		1 0 1 0.12 0 0
CUI: C4275028
Disease: Paternal uniparental disomy of chromosome 20
Paternal uniparental disomy of chromosome 20 		1 0 1 0.12 0 0
CUI: C4304527
Disease: 6q25 microdeletion syndrome
6q25 microdeletion syndrome 		1 0 1 0.12 0 0
CUI: C4476883
Disease: Abnormal pulmonary vein morphology
Abnormal pulmonary vein morphology 		1 0 1 0.12 0 0
CUI: C4546184
Disease: Imprinting error
Imprinting error 		1 0 1 0.12 0 0
CUI: C4551629
Disease: Congenital talipes calcaneovalgus
Congenital talipes calcaneovalgus 		1 0 1 0.12 0 0
CUI: C4707010
Disease: Mosaic trisomy 2 syndrome
Mosaic trisomy 2 syndrome 		1 0 1 0.12 0 0
CUI: C0021833
Disease: Intestinal Fistula
Intestinal Fistula 		2 0 1 0.11 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 0.11 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 0 2 0.25 0 0
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		2 0 1 0.11 0 0
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 0 1 0.11 0 0
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		2 0 1 0.11 0 0
CUI: C1859828
Disease: Increased extraneuronal autofluorescent lipopigment
Increased extraneuronal autofluorescent lipopigment 		2 0 1 0.11 0 0
CUI: C2931746
Disease: Sulfocysteinuria
Sulfocysteinuria 		2 0 1 0.11 0 0
CUI: C2936913
Disease: Porphyria, South African type
Porphyria, South African type 		2 0 1 0.11 0 0
CUI: C3150215
Disease: CHROMOSOME 6q24-q25 DELETION SYNDROME
CHROMOSOME 6q24-q25 DELETION SYNDROME 		2 0 1 0.11 0 0
CUI: C4020917
Disease: Absent fifth fingernail
Absent fifth fingernail 		2 0 1 0.11 0 0
CUI: C4024788
Disease: Anterior chamber synechiae
Anterior chamber synechiae 		2 0 1 0.11 0 0
CUI: C4551590
Disease: Familial renal hypouricemia
Familial renal hypouricemia 		2 0 1 0.11 0 0
CUI: C4551773
Disease: ZIMMERMANN-LABAND SYNDROME 1
ZIMMERMANN-LABAND SYNDROME 1 		2 0 2 0.25 0 0
CUI: C0162569
Disease: Hepatoerythropoietic Porphyria
Hepatoerythropoietic Porphyria 		3 0 1 1.0E-01 0 0
CUI: C0266324
Disease: Congenital dilatation of ureter
Congenital dilatation of ureter 		3 0 1 1.0E-01 0 0
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		3 0 1 1.0E-01 0 0
CUI: C1850451
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 1
CEROID LIPOFUSCINOSIS, NEURONAL, 1 		3 0 1 1.0E-01 0 0