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: C4021630
Disease: Broad long bones
Broad long bones 		6 0 2 0.17 0 0
CUI: C4551566
Disease: Equinovarus deformity of foot
Equinovarus deformity of foot 		6 0 2 0.17 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 0.12 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 0.12 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism 		1 0 1 0.12 0 0
CUI: C0409939
Disease: Osteoarthritis of glenohumeral joint
Osteoarthritis of glenohumeral joint 		1 0 1 0.12 0 0
CUI: C0553668
Disease: Labored breathing
Labored breathing 		1 0 1 0.12 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 0.12 0 0
CUI: C1834056
Disease: Thin anteverted nares
Thin anteverted nares 		1 0 1 0.12 0 0
CUI: C1834057
Disease: Vertebral hyperostosis
Vertebral hyperostosis 		1 0 1 0.12 0 0
CUI: C1835101
Disease: Wide tufts of distal phalanges
Wide tufts of distal phalanges 		1 0 1 0.12 0 0
CUI: C1842531
Disease: Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp 		1 0 1 0.12 0 0
CUI: C1849540
Disease: Delayed eruption of permanent teeth
Delayed eruption of permanent teeth 		10 0 2 0.12 0 0
CUI: C1854061
Disease: Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness 		1 0 1 0.12 0 0
CUI: C1856778
Disease: Widely patent coronal suture
Widely patent coronal suture 		1 0 1 0.12 0 0
CUI: C1857500
Disease: Broad alveolar ridges
Broad alveolar ridges 		10 0 2 0.12 0 0
CUI: C1857508
Disease: Patchy sclerosis of finger phalanx
Patchy sclerosis of finger phalanx 		1 0 1 0.12 0 0
CUI: C1861366
Disease: SYNDACTYLY, TYPE III
SYNDACTYLY, TYPE III 		1 0 1 0.12 0 0
CUI: C1863093
Disease: Alopecia congenita keratosis palmoplantaris
Alopecia congenita keratosis palmoplantaris 		1 0 1 0.12 0 0
CUI: C2678051
Disease: MENTAL RETARDATION, X-LINKED 94 (disorder)
MENTAL RETARDATION, X-LINKED 94 (disorder) 		1 0 1 0.12 0 0
CUI: C2749477
Disease: Oculodentodigital Dysplasia, Autosomal Recessive
Oculodentodigital Dysplasia, Autosomal Recessive 		1 0 1 0.12 0 0
CUI: C2829265
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 86
DEAFNESS, AUTOSOMAL RECESSIVE 86 		1 0 1 0.12 0 0
CUI: C2931577
Disease: Basaran Yilmaz syndrome
Basaran Yilmaz syndrome 		1 0 1 0.12 0 0
CUI: C3151468
Disease: PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1
PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1 		1 0 1 0.12 0 0
CUI: C3275750
Disease: ATRIOVENTRICULAR SEPTAL DEFECT 3
ATRIOVENTRICULAR SEPTAL DEFECT 3 		1 0 1 0.12 0 0