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: C0152427
Disease: Polydactyly
Polydactyly 		188 0 26 0.12 0 0
CUI: C0271270
Disease: Oculovestibuloauditory syndrome
Oculovestibuloauditory syndrome 		87 0 15 0.12 0 0
CUI: C3489733
Disease: Oculomotor apraxia
Oculomotor apraxia 		92 0 15 0.11 0 0
CUI: C4021813
Disease: Oral cleft
Oral cleft 		85 0 14 0.11 0 0
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		46 0 10 0.11 0 0
CUI: C0221217
Disease: Neck webbing
Neck webbing 		78 0 13 0.11 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 9 0.10 0 0
CUI: C1301937
Disease: Talipes
Talipes 		74 0 12 1.0E-01 0 0
CUI: C4023916
Disease: Aplasia/Hypoplasia of the tongue
Aplasia/Hypoplasia of the tongue 		19 0 7 1.0E-01 0 0
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease 		19 0 7 1.0E-01 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 9 9.9E-02 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 25 9.8E-02 0 0
CUI: C1839326
Disease: Abnormal form of the vertebral bodies
Abnormal form of the vertebral bodies 		89 0 13 9.7E-02 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 21 9.6E-02 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 9 9.6E-02 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		137 0 17 9.6E-02 0 0
CUI: C0221365
Disease: Double ureter
Double ureter 		34 0 8 9.5E-02 0 0
CUI: C1610065
Disease: Urethral atresia
Urethral atresia 		23 0 7 9.5E-02 0 0
CUI: C0026010
Disease: Microphthalmos
Microphthalmos 		337 0 34 9.4E-02 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly 		59 0 10 9.3E-02 0 0
CUI: C0265677
Disease: Congenital hemivertebra
Congenital hemivertebra 		49 0 9 9.2E-02 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		27 0 7 9.0E-02 0 0
CUI: C1834129
Disease: Abnormal vertebral morphology
Abnormal vertebral morphology 		28 0 7 8.9E-02 0 0
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1 		53 0 9 8.8E-02 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 13 8.7E-02 0 0