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: C4551474
Disease: Seckel syndrome 1
Seckel syndrome 1 		3 0 2 0.22 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: C0241633
Disease: Vaginal dryness
Vaginal dryness 		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: C0796046
Disease: Gurrieri Sammito Bellussi syndrome
Gurrieri Sammito Bellussi syndrome 		1 0 1 0.12 0 0
CUI: C1302999
Disease: Ankyloblepharon filiforme adnatum
Ankyloblepharon filiforme adnatum 		1 0 1 0.12 0 0
CUI: C1449718
Disease: Endocrine Breast Diseases
Endocrine Breast Diseases 		1 0 1 0.12 0 0
CUI: C1832162
Disease: HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY
HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY 		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: C1844516
Disease: Increased density of long bone diaphyses
Increased density of long bone diaphyses 		1 0 1 0.12 0 0
CUI: C1844519
Disease: Partial fusion of carpals
Partial fusion of carpals 		1 0 1 0.12 0 0
CUI: C1844520
Disease: Partial fusion of tarsals
Partial fusion of tarsals 		1 0 1 0.12 0 0
CUI: C1844702
Disease: Vertical clivus
Vertical clivus 		1 0 1 0.12 0 0
CUI: C1844712
Disease: Nonossified fifth metatarsal
Nonossified fifth metatarsal 		1 0 1 0.12 0 0
CUI: C1845235
Disease: Heterotopia, Periventricular, Ehlers-Danlos Variant
Heterotopia, Periventricular, Ehlers-Danlos Variant 		1 0 1 0.12 0 0
CUI: C1846129
Disease: Terminal Osseous Dysplasia and Pigmentary Defects
Terminal Osseous Dysplasia and Pigmentary Defects 		1 0 1 0.12 0 0
CUI: C1851878
Disease: OROFACIAL CLEFT 8
OROFACIAL CLEFT 8 		1 0 1 0.12 0 0
CUI: C1851885
Disease: Progressive alopecia
Progressive alopecia 		1 0 1 0.12 0 0
CUI: C1856911
Disease: Ivory epiphyses
Ivory epiphyses 		1 0 1 0.12 0 0
CUI: C1857041
Disease: Ectodermal dysplasia, ectrodactyly, and macular dystrophy
Ectodermal dysplasia, ectrodactyly, and macular dystrophy 		1 0 1 0.12 0 0
CUI: C1857508
Disease: Patchy sclerosis of finger phalanx
Patchy sclerosis of finger phalanx 		1 0 1 0.12 0 0