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: C0334619
Disease: HODGKIN'S AND NON-HODGKIN'S LYMPHOMA
HODGKIN'S AND NON-HODGKIN'S LYMPHOMA 		17 0 1 5.6E-02 0 0
CUI: C0751617
Disease: Semilobar Holoprosencephaly
Semilobar Holoprosencephaly 		17 0 1 5.6E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 8 2 5.1E-02 1 6.7E-02
CUI: C1840235
Disease: SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR 		20 0 1 4.8E-02 0 0
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		21 0 1 4.5E-02 0 0
CUI: C0431376
Disease: Cobblestone Lissencephaly
Cobblestone Lissencephaly 		23 0 1 4.2E-02 0 0
CUI: C1610065
Disease: Urethral atresia
Urethral atresia 		23 0 1 4.2E-02 0 0
CUI: C1405984
Disease: Absent radius
Absent radius 		24 0 1 4.0E-02 0 0
CUI: C1832117
Disease: Short humerus
Short humerus 		24 0 1 4.0E-02 0 0
CUI: C4021789
Disease: Abnormality of the vertebral column
Abnormality of the vertebral column 		24 0 1 4.0E-02 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 2 3.6E-02 0 0
CUI: C0542518
Disease: Enlarged kidney
Enlarged kidney 		27 0 1 3.6E-02 0 0
CUI: C1834129
Disease: Abnormal vertebral morphology
Abnormal vertebral morphology 		28 0 1 3.4E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 3.3E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 3.3E-02 0 0
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels 		61 0 2 3.3E-02 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 3.2E-02 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 1 3.2E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 1 3.2E-02 0 0
CUI: C1865572
Disease: Proximal placement of thumb
Proximal placement of thumb 		32 0 1 3.0E-02 0 0
CUI: C0078982
Disease: Arhinencephaly
Arhinencephaly 		35 0 1 2.8E-02 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		35 0 1 2.8E-02 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 1 2.6E-02 0 0
CUI: C0266174
Disease: Duodenal atresia
Duodenal atresia 		39 0 1 2.5E-02 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 1 2.5E-02 0 0