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: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		16 0 16 0.43 0 0
CUI: C0751617
Disease: Semilobar Holoprosencephaly
Semilobar Holoprosencephaly 		17 0 16 0.42 0 0
CUI: C1840238
Disease: Midnasal stenosis
Midnasal stenosis 		16 0 15 0.39 0 0
CUI: C4023916
Disease: Aplasia/Hypoplasia of the tongue
Aplasia/Hypoplasia of the tongue 		19 0 15 0.37 0 0
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease 		19 0 15 0.37 0 0
CUI: C1840235
Disease: SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR 		20 0 15 0.36 0 0
CUI: C1610065
Disease: Urethral atresia
Urethral atresia 		23 0 15 0.33 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 15 0.31 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		27 0 15 0.31 0 0
CUI: C0266174
Disease: Duodenal atresia
Duodenal atresia 		39 0 17 0.29 0 0
CUI: C0221365
Disease: Double ureter
Double ureter 		34 0 15 0.27 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		35 0 15 0.26 0 0
CUI: C0040412
Disease: Fissured tongue
Fissured tongue 		36 0 15 0.26 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 15 0.26 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 16 0.26 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 16 0.25 0 0
CUI: C0158683
Disease: Polycystic liver disease
Polycystic liver disease 		38 0 15 0.25 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1 		49 0 16 0.23 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 15 0.22 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris 		52 0 16 0.22 0 0
CUI: C4551564
Disease: Narrow nasal bridge
Narrow nasal bridge 		47 0 15 0.22 0 0
CUI: C0238395
Disease: Male Pseudohermaphroditism
Male Pseudohermaphroditism 		50 0 15 0.21 0 0
CUI: C1855340
Disease: Bowing of the long bones
Bowing of the long bones 		63 0 17 0.20 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly 		59 0 15 0.19 0 0
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1 		53 0 14 0.18 0 0