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: C0266429
Disease: Monorchism
Monorchism
1 0 1 1.0E-01 0 0
CUI: C0406727
Disease: Orofaciodigital syndrome 4
Orofaciodigital syndrome 4
1 0 1 1.0E-01 0 0
FANCONI ANEMIA, COMPLEMENTATION GROUP B
1 0 1 1.0E-01 0 0
Vater Association With Hydrocephalus
1 0 1 1.0E-01 0 0
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2
1 0 1 1.0E-01 0 0
CUI: C3151113
Disease: MEIER-GORLIN SYNDROME 3
MEIER-GORLIN SYNDROME 3
1 0 1 1.0E-01 0 0
CUI: C3151120
Disease: MEIER-GORLIN SYNDROME 4
MEIER-GORLIN SYNDROME 4
1 0 1 1.0E-01 0 0
CUI: C3151126
Disease: MEIER-GORLIN SYNDROME 5
MEIER-GORLIN SYNDROME 5
1 0 1 1.0E-01 0 0
CUI: C3550331
Disease: Aged leonine appearance
Aged leonine appearance
1 0 1 1.0E-01 0 0
CUI: C3550336
Disease: Multiple rows of eyelashes
Multiple rows of eyelashes
1 0 1 1.0E-01 0 0
CUI: C3553758
Disease: JOUBERT SYNDROME 18
JOUBERT SYNDROME 18
1 0 1 1.0E-01 0 0
CUI: C4021185
Disease: Absent crus of helix
Absent crus of helix
1 0 1 1.0E-01 0 0
CUI: C4021589
Disease: Absent glenoid fossa
Absent glenoid fossa
1 0 1 1.0E-01 0 0
Abnormality of the middle phalanx of the 5th finger
1 0 1 1.0E-01 0 0
Abnormality of male external genitalia
1 0 1 1.0E-01 0 0
CUI: C4225188
Disease: MEIER-GORLIN SYNDROME 6
MEIER-GORLIN SYNDROME 6
1 0 1 1.0E-01 0 0
CUI: C4280330
Disease: Coronal synostosis
Coronal synostosis
1 0 1 1.0E-01 0 0
CUI: C4305002
Disease: VACTERL syndrome with hydrocephalus
VACTERL syndrome with hydrocephalus
1 0 1 1.0E-01 0 0
CUI: C4310738
Disease: MEIER-GORLIN SYNDROME 7
MEIER-GORLIN SYNDROME 7
1 0 1 1.0E-01 0 0
CUI: C4552001
Disease: MEIER-GORLIN SYNDROME 1
MEIER-GORLIN SYNDROME 1
1 0 1 1.0E-01 0 0
CUI: C0235956
Disease: Absence attacks
Absence attacks
2 0 1 9.1E-02 0 0
Chronic lymphocytic leukaemia stage 3
2 0 1 9.1E-02 0 0
Recurrent Adult Acute Lymphoblastic Leukemia
2 0 1 9.1E-02 0 0
CUI: C0549173
Disease: Congenital atresia of rectum
Congenital atresia of rectum
2 0 1 9.1E-02 0 0
CUI: C0561921
Disease: Perineal fistula
Perineal fistula
2 0 1 9.1E-02 0 0