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: C0002831
Disease: Ancylostomiasis
Ancylostomiasis 		1 0 1 0.25 0 0
CUI: C0311386
Disease: Isosporiasis
Isosporiasis 		1 0 1 0.25 0 0
CUI: C0341154
Disease: Esophageal atresia with tracheoesophageal fistula (disorder)
Esophageal atresia with tracheoesophageal fistula (disorder) 		1 0 1 0.25 0 0
CUI: C1845108
Disease: Prominent median palatal raphe
Prominent median palatal raphe 		1 0 1 0.25 0 0
CUI: C1968843
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder) 		1 0 1 0.25 0 0
CUI: C3839990
Disease: Congenital stenosis of nasal pyriform aperture
Congenital stenosis of nasal pyriform aperture 		1 0 1 0.25 0 0
CUI: C0016696
Disease: Freemartin
Freemartin 		2 0 1 0.20 0 0
CUI: C0265581
Disease: Longitudinal deficiency of radius
Longitudinal deficiency of radius 		2 0 1 0.20 0 0
CUI: C0265740
Disease: Arrhinia
Arrhinia 		2 0 1 0.20 0 0
CUI: C0266981
Disease: Torus palatinus
Torus palatinus 		2 0 1 0.20 0 0
CUI: C0585136
Disease: Gastric retention
Gastric retention 		2 0 1 0.20 0 0
CUI: C1542327
Disease: Fetus or newborn affected by alcohol transmitted via placenta or breast milk
Fetus or newborn affected by alcohol transmitted via placenta or breast milk 		2 0 1 0.20 0 0
CUI: C1834877
Disease: HOLOPROSENCEPHALY 2 (disorder)
HOLOPROSENCEPHALY 2 (disorder) 		2 12 1 0.20 2 4.3E-02
CUI: C1856892
Disease: Facial Dysmorphism with Multiple Malformations
Facial Dysmorphism with Multiple Malformations 		2 0 1 0.20 0 0
CUI: C3276742
Disease: Fibular duplication
Fibular duplication 		2 0 1 0.20 0 0
CUI: C4024338
Disease: Deviation of the hand or of fingers of the hand
Deviation of the hand or of fingers of the hand 		2 0 1 0.20 0 0
CUI: C4025390
Disease: Abnormality of the trapezium
Abnormality of the trapezium 		2 0 1 0.20 0 0
CUI: C4025397
Disease: Abnormality of the scaphoid
Abnormality of the scaphoid 		2 0 1 0.20 0 0
CUI: C0431414
Disease: Sacral dysgenesis
Sacral dysgenesis 		3 0 1 0.17 0 0
CUI: C0795803
Disease: Chromosome 2, trisomy 2p
Chromosome 2, trisomy 2p 		3 0 1 0.17 0 0
CUI: C1707400
Disease: Classic medulloblastoma
Classic medulloblastoma 		3 0 1 0.17 0 0
CUI: C1840528
Disease: HOLOPROSENCEPHALY 4 (disorder)
HOLOPROSENCEPHALY 4 (disorder) 		3 0 1 0.17 0 0
CUI: C1861355
Disease: Syndactyly, Type IV
Syndactyly, Type IV 		3 0 1 0.17 0 0
CUI: C1861360
Disease: 6 metacarpals
6 metacarpals 		3 0 1 0.17 0 0
CUI: C1864827
Disease: HOLOPROSENCEPHALY 5
HOLOPROSENCEPHALY 5 		3 0 1 0.17 0 0