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: C4023916
Disease: Aplasia/Hypoplasia of the tongue
Aplasia/Hypoplasia of the tongue
19 0 1 5.3E-02 0 0
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease
19 0 1 5.3E-02 0 0
CUI: C1610065
Disease: Urethral atresia
Urethral atresia
23 0 1 4.3E-02 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome
26 0 1 3.8E-02 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder)
27 0 1 3.7E-02 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
33 0 1 3.0E-02 0 0
CUI: C0221365
Disease: Double ureter
Double ureter
34 0 1 2.9E-02 0 0
CUI: C2675021
Disease: Narrow palpebral fissure
Narrow palpebral fissure
34 0 1 2.9E-02 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI
35 0 1 2.9E-02 0 0
CUI: C0040412
Disease: Fissured tongue
Fissured tongue
36 0 1 2.8E-02 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 1 2.8E-02 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly
37 0 1 2.7E-02 0 0
CUI: C0158683
Disease: Polycystic liver disease
Polycystic liver disease
38 0 1 2.6E-02 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen
41 0 1 2.4E-02 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea
42 0 1 2.4E-02 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 1 2.2E-02 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1
49 0 1 2.0E-02 0 0
CUI: C0238395
Disease: Male Pseudohermaphroditism
Male Pseudohermaphroditism
50 0 1 2.0E-02 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris
52 0 1 1.9E-02 0 0
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1
53 38 1 1.9E-02 1 2.4E-02
CUI: C0002902
Disease: Anencephaly
Anencephaly
59 0 1 1.7E-02 0 0
CUI: C0030283
Disease: Pancreatic Cyst
Pancreatic Cyst
60 0 1 1.7E-02 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
61 0 1 1.6E-02 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital
63 0 1 1.6E-02 0 0
CUI: C1855340
Disease: Bowing of the long bones
Bowing of the long bones
63 0 1 1.6E-02 0 0