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: C4021592
Disease: Unilateral primary pulmonary dysgenesis
Unilateral primary pulmonary dysgenesis 		5 0 1 0.17 0 0
CUI: C4024669
Disease: Asymmetry of spinal facet joints
Asymmetry of spinal facet joints 		5 0 1 0.17 0 0
CUI: C0265291
Disease: Kenny-Caffey syndrome
Kenny-Caffey syndrome 		6 0 1 0.14 0 0
CUI: C1836929
Disease: Emanuel syndrome
Emanuel syndrome 		6 0 1 0.14 0 0
CUI: C1837341
Disease: Transposition of the Great Arteries, Dextro-Looped 1
Transposition of the Great Arteries, Dextro-Looped 1 		6 0 1 0.14 0 0
CUI: C1960883
Disease: Spina bifida aperta of cervical spine
Spina bifida aperta of cervical spine 		6 0 1 0.14 0 0
CUI: C4023796
Disease: Aplasia/Hypoplasia of the thymus
Aplasia/Hypoplasia of the thymus 		6 0 1 0.14 0 0
CUI: C0344490
Disease: Sacral agenesis
Sacral agenesis 		15 0 2 0.13 0 0
CUI: C0019296
Disease: Inguinal Hernia, Indirect
Inguinal Hernia, Indirect 		7 0 1 0.12 0 0
CUI: C4025695
Disease: Right aortic arch with mirror image branching
Right aortic arch with mirror image branching 		7 0 1 0.12 0 0
CUI: C0013447
Disease: Ear Diseases
Ear Diseases 		8 0 1 0.11 0 0
CUI: C1866994
Disease: Ulnar-mammary syndrome
Ulnar-mammary syndrome 		8 0 1 0.11 0 0
CUI: C1859101
Disease: Vertebral chordoma
Vertebral chordoma 		9 0 1 1.0E-01 0 0
CUI: C4024912
Disease: Occipital myelomeningocele
Occipital myelomeningocele 		9 0 1 1.0E-01 0 0
CUI: C0392485
Disease: Congenital diverticulum of pharynx
Congenital diverticulum of pharynx 		10 0 1 9.1E-02 0 0
CUI: C1845052
Disease: AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1 		10 0 1 9.1E-02 0 0
CUI: C1264041
Disease: von Willebrand Disease, Type 3
von Willebrand Disease, Type 3 		11 0 1 8.3E-02 0 0
CUI: C3891448
Disease: NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO 		11 0 1 8.3E-02 0 0
CUI: C0300948
Disease: Caudal Regression Syndrome
Caudal Regression Syndrome 		12 0 1 7.7E-02 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome 		12 0 1 7.7E-02 0 0
CUI: C4021161
Disease: Multiple suture craniosynostosis
Multiple suture craniosynostosis 		12 0 1 7.7E-02 0 0
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils 		12 0 1 7.7E-02 0 0
CUI: C0013743
Disease: Eisenmenger Complex
Eisenmenger Complex 		13 0 1 7.1E-02 0 0
CUI: C0152419
Disease: Interrupted aortic arch
Interrupted aortic arch 		13 0 1 7.1E-02 0 0
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		13 0 1 7.1E-02 0 0