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: C0017567
Disease: Gingival Hypertrophy
Gingival Hypertrophy 		7 0 3 0.15 0 0
CUI: C0221775
Disease: Lumbar disc disease
Lumbar disc disease 		49 30 8 0.14 1 3.3E-02
CUI: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease 		41 83 7 0.14 1 1.2E-02
CUI: C0878693
Disease: Conjunctivochalasis
Conjunctivochalasis 		9 0 3 0.14 0 0
CUI: C0157946
Disease: Osteoarthrosis, localized, not specified whether primary or secondary
Osteoarthrosis, localized, not specified whether primary or secondary 		28 0 5 0.13 0 0
CUI: C0231586
Disease: Joint function disorder
Joint function disorder 		2 0 2 0.12 0 0
CUI: C0265235
Disease: Marshall syndrome
Marshall syndrome 		2 0 2 0.12 0 0
CUI: C1096253
Disease: Cardiac infection
Cardiac infection 		2 0 2 0.12 0 0
CUI: C4025356
Disease: Abnormal vitreous humor morphology
Abnormal vitreous humor morphology 		2 0 2 0.12 0 0
CUI: C0263874
Disease: Degeneration of lumbar intervertebral disc
Degeneration of lumbar intervertebral disc 		50 0 7 0.12 0 0
CUI: C0155366
Disease: Vitreous degeneration
Vitreous degeneration 		3 0 2 0.12 0 0
CUI: C0282008
Disease: Dilation of the thoracic aorta
Dilation of the thoracic aorta 		3 0 2 0.12 0 0
CUI: C0349516
Disease: Isolated aortic stenosis
Isolated aortic stenosis 		3 0 2 0.12 0 0
CUI: C0423747
Disease: Deep pain on intercourse
Deep pain on intercourse 		3 0 2 0.12 0 0
CUI: C1333843
Disease: Grade 3 Invasive Breast Carcinoma
Grade 3 Invasive Breast Carcinoma 		3 0 2 0.12 0 0
CUI: C1848488
Disease: Pierre Robin syndrome with fetal chondrodysplasia
Pierre Robin syndrome with fetal chondrodysplasia 		3 0 2 0.12 0 0
CUI: C4025424
Disease: Abnormality of ulnar metaphysis
Abnormality of ulnar metaphysis 		3 0 2 0.12 0 0
CUI: C0007302
Disease: Cartilage Diseases
Cartilage Diseases 		23 0 4 0.11 0 0
CUI: C0154051
Disease: Hemangioma of retina
Hemangioma of retina 		4 0 2 0.11 0 0
CUI: C1858084
Disease: STICKLER SYNDROME, TYPE II (disorder)
STICKLER SYNDROME, TYPE II (disorder) 		4 0 2 0.11 0 0
CUI: C2749582
Disease: Dumbbell-shaped long bone
Dumbbell-shaped long bone 		4 0 2 0.11 0 0
CUI: C0432211
Disease: Spondyloepimetaphyseal disorder
Spondyloepimetaphyseal disorder 		37 0 5 0.10 0 0
CUI: C0339229
Disease: Superior limbic keratoconjunctivitis
Superior limbic keratoconjunctivitis 		6 0 2 1.0E-01 0 0
CUI: C0341299
Disease: Collagenous Sprue
Collagenous Sprue 		6 0 2 1.0E-01 0 0
CUI: C0700635
Disease: Strudwick syndrome
Strudwick syndrome 		17 0 3 1.0E-01 0 0