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: C0426799
Disease: Congenital hypoplasia of clavicle
Congenital hypoplasia of clavicle 		28 0 5 6.7E-02 0 0
CUI: C1740827
Disease: CLL progression
CLL progression 		28 0 5 6.7E-02 0 0
CUI: C0276926
Disease: Schistosoma hematobium infection
Schistosoma hematobium infection 		13 0 4 6.6E-02 0 0
CUI: C0035934
Disease: Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome 		31 0 5 6.4E-02 0 0
CUI: C1336735
Disease: Treatment related acute myeloid leukaemia
Treatment related acute myeloid leukaemia 		65 0 7 6.4E-02 0 0
CUI: C0033300
Disease: Progeria
Progeria 		118 0 10 6.2E-02 0 0
CUI: C0242225
Disease: Color blindness
Color blindness 		33 0 5 6.2E-02 0 0
CUI: C1266157
Disease: Intratubular malignant germ cells
Intratubular malignant germ cells 		16 0 4 6.2E-02 0 0
CUI: C0206661
Disease: Gonadoblastoma
Gonadoblastoma 		34 0 5 6.2E-02 0 0
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		18 0 4 6.1E-02 0 0
CUI: C0740985
Disease: Acute anaemia
Acute anaemia 		18 0 4 6.1E-02 0 0
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding) 		18 0 4 6.1E-02 0 0
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome 		94 0 8 5.8E-02 0 0
CUI: C1334680
Disease: Mediastinal seminoma
Mediastinal seminoma 		3 0 3 5.8E-02 0 0
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis 		40 0 5 5.7E-02 0 0
CUI: C0043154
Disease: Dental White Spot
Dental White Spot 		22 0 4 5.7E-02 0 0
CUI: C0031029
Disease: Periapical Granuloma
Periapical Granuloma 		41 0 5 5.7E-02 0 0
CUI: C0334518
Disease: Polyembryoma
Polyembryoma 		4 0 3 5.7E-02 0 0
CUI: C0280141
Disease: Acute Undifferentiated Leukemia
Acute Undifferentiated Leukemia 		119 0 9 5.6E-02 0 0
CUI: C0432292
Disease: Familial expansile osteolysis
Familial expansile osteolysis 		5 0 3 5.6E-02 0 0
CUI: C1704274
Disease: Intrauterine adhesions
Intrauterine adhesions 		24 0 4 5.6E-02 0 0
CUI: C1859569
Disease: BARDET-BIEDL SYNDROME 11
BARDET-BIEDL SYNDROME 11 		5 0 3 5.6E-02 0 0
CUI: C4721411
Disease: Osteolysis
Osteolysis 		62 0 6 5.6E-02 0 0
CUI: C4728047
Disease: Left anterior descending coronary artery occlusion
Left anterior descending coronary artery occlusion 		5 0 3 5.6E-02 0 0
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		158 0 11 5.5E-02 0 0