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: C1837792
Disease: Insulin-resistant diabetes mellitus at puberty
Insulin-resistant diabetes mellitus at puberty 		5 0 2 0.22 0 0
CUI: C4023965
Disease: Structural foot deformity
Structural foot deformity 		5 0 2 0.22 0 0
CUI: C4024993
Disease: Aplasia/Hypoplasia of the clavicles
Aplasia/Hypoplasia of the clavicles 		5 0 2 0.22 0 0
CUI: C1846438
Disease: Hypoplastic facial bones
Hypoplastic facial bones 		6 0 2 0.20 0 0
CUI: C1856542
Disease: Prominent scalp veins
Prominent scalp veins 		6 0 2 0.20 0 0
CUI: C4020957
Disease: Abnormal trabecular bone morphology
Abnormal trabecular bone morphology 		6 0 2 0.20 0 0
CUI: C3810018
Disease: Bilateral coxa valga
Bilateral coxa valga 		7 0 2 0.18 0 0
CUI: C1833325
Disease: Thin bony cortex
Thin bony cortex 		14 0 3 0.18 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 0.17 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 0.17 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 0.17 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 0.17 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 0.17 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 0.17 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 0.17 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 0.17 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 0.17 0 0
CUI: C0865573
Disease: Mitral disease
Mitral disease 		1 0 1 0.17 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 0.17 0 0
CUI: C1832942
Disease: JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder) 		1 0 1 0.17 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 0.17 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 0.17 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 0.17 0 0
CUI: C1837756
Disease: MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY 		1 0 1 0.17 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 0.17 0 0