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: C0270805
Disease: Hemiplegic cerebral palsy
Hemiplegic cerebral palsy 		1 0 1 7.7E-02 0 0
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		1 0 1 7.7E-02 0 0
CUI: C0340235
Disease: Bronchobiliary fistula
Bronchobiliary fistula 		1 0 1 7.7E-02 0 0
CUI: C0343081
Disease: Livedoid vasculitis
Livedoid vasculitis 		1 0 1 7.7E-02 0 0
CUI: C0519055
Disease: Renal involvement in scleroderma
Renal involvement in scleroderma 		1 0 1 7.7E-02 0 0
CUI: C0544852
Disease: Hypertrichosis, universal
Hypertrichosis, universal 		1 0 1 7.7E-02 0 0
CUI: C0589110
Disease: Postoperative deep vein thrombosis
Postoperative deep vein thrombosis 		1 0 1 7.7E-02 0 0
CUI: C0854142
Disease: Thrombosis of aorta
Thrombosis of aorta 		1 0 1 7.7E-02 0 0
CUI: C0948048
Disease: Malignant neoplasm progression
Malignant neoplasm progression 		1 0 1 7.7E-02 0 0
CUI: C1397674
Disease: Persistent foramen ovale
Persistent foramen ovale 		1 0 1 7.7E-02 0 0
CUI: C1709573
Disease: Pleural Epithelioid Hemangioendothelioma
Pleural Epithelioid Hemangioendothelioma 		1 0 1 7.7E-02 0 0
CUI: C1837149
Disease: Alzheimer Disease 9
Alzheimer Disease 9 		1 0 1 7.7E-02 0 0
CUI: C1853831
Disease: Bleeding Disorder, East Texas Type
Bleeding Disorder, East Texas Type 		1 0 1 7.7E-02 0 0
CUI: C1854061
Disease: Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness 		1 0 1 7.7E-02 0 0
CUI: C1855000
Disease: Agenesis of central incisor
Agenesis of central incisor 		1 0 1 7.7E-02 0 0
CUI: C1859458
Disease: Cleft vertebral arch
Cleft vertebral arch 		1 0 1 7.7E-02 0 0
CUI: C1859462
Disease: Absent knee epiphyses
Absent knee epiphyses 		1 0 1 7.7E-02 0 0
CUI: C2676744
Disease: BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO
BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO 		1 0 1 7.7E-02 0 0
CUI: C2930802
Disease: Familial antiphospholipid syndrome
Familial antiphospholipid syndrome 		1 0 1 7.7E-02 0 0
CUI: C2931889
Disease: Oral-facial-digital syndrome, type 2
Oral-facial-digital syndrome, type 2 		1 0 1 7.7E-02 0 0
CUI: C3280670
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1 		1 0 1 7.7E-02 0 0
CUI: C3553661
Disease: CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION 		1 0 1 7.7E-02 0 0
CUI: C3806516
Disease: Disproportionate shortening of the tibia
Disproportionate shortening of the tibia 		1 0 1 7.7E-02 0 0
CUI: C4017271
Disease: factor V Hong Kong phenotype
factor V Hong Kong phenotype 		1 0 1 7.7E-02 0 0
CUI: C4021336
Disease: Complete duplication of hallux phalanx
Complete duplication of hallux phalanx 		1 0 1 7.7E-02 0 0