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: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome 		11 0 8 0.24 0 0
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		35 0 11 0.20 0 0
CUI: C2674219
Disease: SPHEROCYTOSIS, HEREDITARY, 2
SPHEROCYTOSIS, HEREDITARY, 2 		8 0 5 0.15 0 0
CUI: C1855496
Disease: Contiguous gene syndrome
Contiguous gene syndrome 		52 0 9 0.12 0 0
CUI: C0795940
Disease: Filippi syndrome
Filippi syndrome 		6 0 4 0.12 0 0
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		29 0 6 0.11 0 0
CUI: C3887980
Disease: Protanomaly
Protanomaly 		19 0 5 0.11 0 0
CUI: C0036211
Disease: Sarcoma 180
Sarcoma 180 		20 0 5 0.11 0 0
CUI: C3831784
Disease: Acute monocytic/monoblastic leukemia
Acute monocytic/monoblastic leukemia 		35 0 6 1.0E-01 0 0
CUI: C0344191
Disease: Cerebellar decompression injury
Cerebellar decompression injury 		14 0 4 9.8E-02 0 0
CUI: C0457334
Disease: Acute monoblastic leukemia
Acute monoblastic leukemia 		37 0 6 9.7E-02 0 0
CUI: C4076240
Disease: Chronic kidney disease mineral and bone disorder
Chronic kidney disease mineral and bone disorder 		26 0 5 9.6E-02 0 0
CUI: C0729582
Disease: Floating-harbor syndrome
Floating-harbor syndrome 		4 0 3 9.4E-02 0 0
CUI: C1096527
Disease: Mosaic trisomy 8 syndrome
Mosaic trisomy 8 syndrome 		4 0 3 9.4E-02 0 0
CUI: C0948391
Disease: Convulsion in childhood
Convulsion in childhood 		5 0 3 9.1E-02 0 0
CUI: C4021395
Disease: Abnormality of the antihelix
Abnormality of the antihelix 		17 0 4 9.1E-02 0 0
CUI: C1292780
Disease: Therapy-related myelodysplastic syndrome
Therapy-related myelodysplastic syndrome 		42 0 6 9.0E-02 0 0
CUI: C2825306
Disease: Treatment related leukaemia
Treatment related leukaemia 		30 0 5 8.9E-02 0 0
CUI: C1860164
Disease: Duplication of phalanx of hallux
Duplication of phalanx of hallux 		6 0 3 8.8E-02 0 0
CUI: C1302790
Disease: Congenital malformation syndrome
Congenital malformation syndrome 		57 0 7 8.6E-02 0 0
CUI: C0242225
Disease: Color blindness
Color blindness 		33 0 5 8.5E-02 0 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		73 0 8 8.3E-02 0 0
CUI: C1970431
Disease: PITT-HOPKINS SYNDROME
PITT-HOPKINS SYNDROME 		9 0 3 8.1E-02 0 0
CUI: C0234853
Disease: Facial grimacing
Facial grimacing 		10 0 3 7.9E-02 0 0
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis 		40 0 5 7.6E-02 0 0