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: C0241397
Disease: Triphalangeal thumb
Triphalangeal thumb
56 0 10 0.10 0 0
Congenital absence of kidneys syndrome
110 0 15 0.10 0 0
CUI: C0431663
Disease: Bilateral Cryptorchidism
Bilateral Cryptorchidism
48 0 9 1.0E-01 0 0
CUI: C0426817
Disease: Short ribs
Short ribs
60 0 10 9.9E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
95 0 13 9.8E-02 0 0
CUI: C0265660
Disease: Syndactyly of the toes
Syndactyly of the toes
129 0 16 9.8E-02 0 0
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I
17 0 6 9.7E-02 0 0
CUI: C0220769
Disease: FG syndrome
FG syndrome
19 0 6 9.4E-02 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers
92 0 12 9.2E-02 0 0
CUI: C0025995
Disease: Micromelia
Micromelia
104 0 13 9.2E-02 0 0
Aplasia/Hypoplasia of the corpus callosum
108 0 13 8.9E-02 0 0
CUI: C1859717
Disease: Depressed nasal tip
Depressed nasal tip
23 0 6 8.8E-02 0 0
CUI: C1405984
Disease: Absent radius
Absent radius
24 0 6 8.7E-02 0 0
CUI: C4021814
Disease: Accessory oral frenulum
Accessory oral frenulum
12 0 5 8.6E-02 0 0
Progressive pseudorheumatoid dysplasia
64 0 9 8.5E-02 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow
141 0 15 8.5E-02 0 0
Greig cephalopolysyndactyly syndrome
14 0 5 8.3E-02 0 0
CUI: C1850256
Disease: Median cleft lip
Median cleft lip
15 0 5 8.2E-02 0 0
CUI: C1850259
Disease: Short tibia
Short tibia
17 0 5 7.9E-02 0 0
CUI: C0206762
Disease: Limb Deformities, Congenital
Limb Deformities, Congenital
59 0 8 7.8E-02 0 0
CUI: C0920652
Disease: skin irritant
skin irritant
4 0 4 7.8E-02 0 0
CUI: C1867131
Disease: Broad hallux
Broad hallux
48 0 7 7.6E-02 0 0
CUI: C0026363
Disease: Mohr Syndrome
Mohr Syndrome
6 0 4 7.5E-02 0 0
CUI: C1846474
Disease: Small thenar eminence
Small thenar eminence
6 0 4 7.5E-02 0 0
CUI: C0265654
Disease: Tarsal Coalition
Tarsal Coalition
22 0 5 7.4E-02 0 0