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: C1845292
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP B
FANCONI ANEMIA, COMPLEMENTATION GROUP B 		1 0 1 9.1E-02 0 0
CUI: C1848600
Disease: Vater Association With Hydrocephalus
Vater Association With Hydrocephalus 		1 0 1 9.1E-02 0 0
CUI: C2676772
Disease: Microtia, Hearing Impairment, And Cleft Palate
Microtia, Hearing Impairment, And Cleft Palate 		1 0 1 9.1E-02 0 0
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		1 0 1 9.1E-02 0 0
CUI: C3151113
Disease: MEIER-GORLIN SYNDROME 3
MEIER-GORLIN SYNDROME 3 		1 0 1 9.1E-02 0 0
CUI: C3151120
Disease: MEIER-GORLIN SYNDROME 4
MEIER-GORLIN SYNDROME 4 		1 0 1 9.1E-02 0 0
CUI: C3151126
Disease: MEIER-GORLIN SYNDROME 5
MEIER-GORLIN SYNDROME 5 		1 0 1 9.1E-02 0 0
CUI: C3808166
Disease: MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT
MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT 		1 0 1 9.1E-02 0 0
CUI: C4021589
Disease: Absent glenoid fossa
Absent glenoid fossa 		1 0 1 9.1E-02 0 0
CUI: C4025406
Disease: Abnormality of the middle phalanx of the 5th finger
Abnormality of the middle phalanx of the 5th finger 		1 0 1 9.1E-02 0 0
CUI: C4225188
Disease: MEIER-GORLIN SYNDROME 6
MEIER-GORLIN SYNDROME 6 		1 0 1 9.1E-02 0 0
CUI: C4280330
Disease: Coronal synostosis
Coronal synostosis 		1 0 1 9.1E-02 0 0
CUI: C4305002
Disease: VACTERL syndrome with hydrocephalus
VACTERL syndrome with hydrocephalus 		1 0 1 9.1E-02 0 0
CUI: C4310738
Disease: MEIER-GORLIN SYNDROME 7
MEIER-GORLIN SYNDROME 7 		1 0 1 9.1E-02 0 0
CUI: C4552001
Disease: MEIER-GORLIN SYNDROME 1
MEIER-GORLIN SYNDROME 1 		1 0 1 9.1E-02 0 0
CUI: C4694002
Disease: MICROTIA WITHOUT HEARING IMPAIRMENT
MICROTIA WITHOUT HEARING IMPAIRMENT 		1 0 1 9.1E-02 0 0
CUI: C0235956
Disease: Absence attacks
Absence attacks 		2 0 1 8.3E-02 0 0
CUI: C0278769
Disease: Chronic lymphocytic leukaemia stage 3
Chronic lymphocytic leukaemia stage 3 		2 0 1 8.3E-02 0 0
CUI: C1855177
Disease: Flat glenoid fossa
Flat glenoid fossa 		2 0 1 8.3E-02 0 0
CUI: C2677485
Disease: Aplasia of the sweat glands
Aplasia of the sweat glands 		2 0 1 8.3E-02 0 0
CUI: C2749240
Disease: Vater Association With Macrocephaly And Ventriculomegaly
Vater Association With Macrocephaly And Ventriculomegaly 		2 0 1 8.3E-02 0 0
CUI: C2931228
Disease: VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS 		2 0 1 8.3E-02 0 0
CUI: C4225317
Disease: ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE
ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE 		2 0 1 8.3E-02 0 0
CUI: C0406641
Disease: Genital lichen sclerosus
Genital lichen sclerosus 		3 0 1 7.7E-02 0 0
CUI: C1332156
Disease: Acute myelomonocytic leukemia with abnormal eosinophils
Acute myelomonocytic leukemia with abnormal eosinophils 		3 0 1 7.7E-02 0 0