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: C1862096
Disease: Aplasia of the middle phalanx of the hand
Aplasia of the middle phalanx of the hand 		2 0 1 0.50 0 0
CUI: C4551510
Disease: CARPENTER SYNDROME 1
CARPENTER SYNDROME 1 		2 0 1 0.50 0 0
CUI: C1275078
Disease: Acrocephalopolysyndactyly type 2
Acrocephalopolysyndactyly type 2 		7 0 1 0.14 0 0
CUI: C1860050
Disease: Cloverleaf skull
Cloverleaf skull 		8 0 1 0.12 0 0
CUI: C1855670
Disease: Abnormal cornea morphology
Abnormal cornea morphology 		9 0 1 0.11 0 0
CUI: C2112942
Disease: Preaxial foot polydactyly
Preaxial foot polydactyly 		10 0 1 1.0E-01 0 0
CUI: C1856659
Disease: Polysplenia
Polysplenia 		15 0 1 6.7E-02 0 0
CUI: C4021254
Disease: Cutaneous finger syndactyly
Cutaneous finger syndactyly 		20 0 1 5.0E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 3.4E-02 0 0
CUI: C1855333
Disease: External genital hypoplasia
External genital hypoplasia 		29 0 1 3.4E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 3.4E-02 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 3.3E-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 3.3E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 1 3.3E-02 0 0
CUI: C0432355
Disease: Hypoplasia of nipple
Hypoplasia of nipple 		33 0 1 3.0E-02 0 0
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		35 0 1 2.9E-02 0 0
CUI: C0266011
Disease: Accessory nipple
Accessory nipple 		38 0 1 2.6E-02 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 1 2.6E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 2.6E-02 0 0
CUI: C1398312
Disease: Narrow palate
Narrow palate 		40 0 1 2.5E-02 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 2.4E-02 0 0
CUI: C0238421
Disease: Selenium deficiency
Selenium deficiency 		44 0 1 2.3E-02 0 0
CUI: C0345354
Disease: Radial polydactyly
Radial polydactyly 		51 0 1 2.0E-02 0 0
CUI: C0426891
Disease: Broad thumbs
Broad thumbs 		67 0 1 1.5E-02 0 0
CUI: C0010495
Disease: Cutis Laxa
Cutis Laxa 		70 0 1 1.4E-02 0 0