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: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1
49 0 9 0.16 0 0
CUI: C4022171
Disease: Periauricular skin pits
Periauricular skin pits
5 0 3 0.15 0 0
CUI: C0431420
Disease: Vein of Galen aneurysm
Vein of Galen aneurysm
6 0 3 0.14 0 0
CUI: C0431663
Disease: Bilateral Cryptorchidism
Bilateral Cryptorchidism
48 0 8 0.14 0 0
CUI: C1853406
Disease: Difficulty in tongue movements
Difficulty in tongue movements
8 0 3 0.13 0 0
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing
60 0 9 0.13 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes
61 0 9 0.13 0 0
CUI: C4023916
Disease: Aplasia/Hypoplasia of the tongue
Aplasia/Hypoplasia of the tongue
19 0 4 0.12 0 0
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease
19 0 4 0.12 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
95 0 12 0.12 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
61 0 8 0.11 0 0
Cleft at the superior portion of the pinna
2 0 2 0.11 0 0
CUI: C4021814
Disease: Accessory oral frenulum
Accessory oral frenulum
12 0 3 0.11 0 0
CUI: C1610065
Disease: Urethral atresia
Urethral atresia
23 0 4 0.11 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly
75 0 9 0.11 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome
26 0 4 1.0E-01 0 0
CUI: C1865305
Disease: Hypoplastic superior helix
Hypoplastic superior helix
4 0 2 1.0E-01 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder)
27 0 4 9.8E-02 0 0
Aplasia/Hypoplasia of the corpus callosum
108 0 11 9.6E-02 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers
92 0 9 8.9E-02 0 0
CUI: C0025988
Disease: Microglossia
Microglossia
19 0 3 8.8E-02 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 5 8.6E-02 0 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome
21 0 3 8.3E-02 0 0
CUI: C0221365
Disease: Double ureter
Double ureter
34 0 4 8.3E-02 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia
100 0 9 8.3E-02 0 0