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: C4539714
Disease: MECKEL SYNDROME 13
MECKEL SYNDROME 13 		1 0 1 1.00 0 0
CUI: C4539729
Disease: OROFACIODIGITAL SYNDROME XVI
OROFACIODIGITAL SYNDROME XVI 		1 2 1 1.00 1 0.50
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I 		17 0 1 5.9E-02 0 0
CUI: C0431565
Disease: Hamartoma of tongue
Hamartoma of tongue 		18 0 1 5.6E-02 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes 		19 1 1 5.3E-02 1 1.00
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: C1709353
Disease: Osteofibrous Dysplasia
Osteofibrous Dysplasia 		25 0 1 4.0E-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: C3281200
Disease: LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS
LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS 		33 0 1 3.0E-02 0 0
CUI: C0221365
Disease: Double ureter
Double ureter 		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