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: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		13 0 3 1.0E-01 0 0
CUI: C0341007
Disease: Alveolar ridge abnormality
Alveolar ridge abnormality 		2 0 2 1.0E-01 0 0
CUI: C1834877
Disease: HOLOPROSENCEPHALY 2 (disorder)
HOLOPROSENCEPHALY 2 (disorder) 		2 0 2 1.0E-01 0 0
CUI: C1856892
Disease: Facial Dysmorphism with Multiple Malformations
Facial Dysmorphism with Multiple Malformations 		2 0 2 1.0E-01 0 0
CUI: C1857005
Disease: Cone-shaped epiphyses of phalanges 2 to 5
Cone-shaped epiphyses of phalanges 2 to 5 		2 0 2 1.0E-01 0 0
CUI: C0334482
Disease: Fetal rhabdomyoma
Fetal rhabdomyoma 		3 0 2 9.5E-02 0 0
CUI: C1862304
Disease: Hamartomatous polyp of stomach
Hamartomatous polyp of stomach 		3 0 2 9.5E-02 0 0
CUI: C1866959
Disease: Sella Turcica, Bridged
Sella Turcica, Bridged 		3 0 2 9.5E-02 0 0
CUI: C4020770
Disease: Hypoplasia of the premaxilla
Hypoplasia of the premaxilla 		3 0 2 9.5E-02 0 0
CUI: C4025374
Disease: Irregular ossification of hand bones
Irregular ossification of hand bones 		3 0 2 9.5E-02 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 17 9.2E-02 0 0
CUI: C0155285
Disease: Orbital cyst
Orbital cyst 		4 0 2 9.1E-02 0 0
CUI: C0423776
Disease: Palmar pit
Palmar pit 		4 0 2 9.1E-02 0 0
CUI: C0457013
Disease: Weyers acrofacial dysostosis
Weyers acrofacial dysostosis 		4 0 2 9.1E-02 0 0
CUI: C1096654
Disease: Cardiac fibroma
Cardiac fibroma 		4 0 2 9.1E-02 0 0
CUI: C1334410
Disease: Localized Primitive Neuroectodermal Tumor
Localized Primitive Neuroectodermal Tumor 		4 0 2 9.1E-02 0 0
CUI: C1840529
Disease: HOLOPROSENCEPHALY 3
HOLOPROSENCEPHALY 3 		4 37 2 9.1E-02 2 5.3E-02
CUI: C1852301
Disease: Plantar pits
Plantar pits 		4 0 2 9.1E-02 0 0
CUI: C2931870
Disease: Familial schizencephaly
Familial schizencephaly 		4 0 2 9.1E-02 0 0
CUI: C4053775
Disease: Pituitary stalk interruption syndrome
Pituitary stalk interruption syndrome 		16 0 3 9.1E-02 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 6 8.7E-02 0 0
CUI: C0685682
Disease: Single naris
Single naris 		5 0 2 8.7E-02 0 0
CUI: C3808270
Disease: Acetabular spurs
Acetabular spurs 		5 0 2 8.7E-02 0 0
CUI: C0149951
Disease: Ovarian Fibromata
Ovarian Fibromata 		6 0 2 8.3E-02 0 0
CUI: C0685869
Disease: Monophthalmos
Monophthalmos 		6 0 2 8.3E-02 0 0