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: C0409338
Disease: Flexion contracture - elbow
Flexion contracture - elbow 		73 0 19 0.12 0 0
CUI: C0332878
Disease: Congenital contracture
Congenital contracture 		31 0 14 0.11 0 0
CUI: C1840311
Disease: Laryngeal cleft
Laryngeal cleft 		72 0 17 0.10 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 10 16 0.10 1 4.8E-02
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		54 0 15 1.0E-01 0 0
CUI: C0243050
Disease: Cardiovascular Abnormalities
Cardiovascular Abnormalities 		99 0 19 9.9E-02 0 0
CUI: C3693482
Disease: Giant Cell Fibroblastoma
Giant Cell Fibroblastoma 		77 0 17 9.9E-02 0 0
CUI: C1334386
Disease: Meningeal melanoma
Meningeal melanoma 		23 0 12 9.8E-02 0 0
CUI: C0024106
Disease: Lumpy Skin Disease
Lumpy Skin Disease 		12 0 11 9.8E-02 0 0
CUI: C0857116
Disease: Gross obesity
Gross obesity 		12 0 11 9.8E-02 0 0
CUI: C0580174
Disease: Portal hypertensive gastropathy
Portal hypertensive gastropathy 		24 0 12 9.8E-02 0 0
CUI: C1840348
Disease: Hypocalciuric Hypercalcemia, Acquired
Hypocalciuric Hypercalcemia, Acquired 		13 0 11 9.7E-02 0 0
CUI: C0162810
Disease: Cicatrix, Hypertrophic
Cicatrix, Hypertrophic 		185 0 26 9.6E-02 0 0
CUI: C0162298
Disease: Joint stiffness
Joint stiffness 		163 0 24 9.6E-02 0 0
CUI: C1847352
Disease: POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL 		15 0 11 9.6E-02 0 0
CUI: C0392784
Disease: Dermatofibrosarcoma Protuberans
Dermatofibrosarcoma Protuberans 		78 0 16 9.2E-02 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		198 0 26 9.2E-02 0 0
CUI: C0553665
Disease: Skin endocrine disorder
Skin endocrine disorder 		34 0 12 9.0E-02 0 0
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases 		171 0 23 8.9E-02 0 0
CUI: C0011119
Disease: Decompression Sickness
Decompression Sickness 		98 0 17 8.9E-02 0 0
CUI: C1285162
Disease: Degenerative disorder
Degenerative disorder 		160 0 22 8.8E-02 0 0
CUI: C0342684
Disease: Ocular albinism, type I
Ocular albinism, type I 		38 0 12 8.8E-02 0 0
CUI: C0021122
Disease: Disruptive, Impulse Control, and Conduct Disorders
Disruptive, Impulse Control, and Conduct Disorders 		67 0 14 8.5E-02 0 0
CUI: C0024003
Disease: Lordosis
Lordosis 		160 0 21 8.4E-02 0 0
CUI: C0162770
Disease: Right Ventricular Hypertrophy
Right Ventricular Hypertrophy 		160 0 21 8.4E-02 0 0