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: C0035091
Disease: Renal Tubular Transport, Inborn Errors
Renal Tubular Transport, Inborn Errors 		1 0 1 7.1E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 7.1E-02 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 7.1E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 7.1E-02 0 0
CUI: C0265978
Disease: Collagen nevus of skin
Collagen nevus of skin 		1 0 1 7.1E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 7.1E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 7.1E-02 0 0
CUI: C0271869
Disease: Pseudohypoparathyroidism type I B
Pseudohypoparathyroidism type I B 		1 0 1 7.1E-02 0 0
CUI: C0477611
Disease: [X]Spinal osteochondrosis, unspecified
[X]Spinal osteochondrosis, unspecified 		1 0 1 7.1E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 7.1E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 7.1E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 7.1E-02 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 7.1E-02 0 0
CUI: C0856247
Disease: Lumbar spine degeneration
Lumbar spine degeneration 		1 0 1 7.1E-02 0 0
CUI: C0948755
Disease: Pulmonary failure
Pulmonary failure 		1 0 1 7.1E-02 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 7.1E-02 0 0
CUI: C1313977
Disease: Dental cyst
Dental cyst 		1 0 1 7.1E-02 0 0
CUI: C1321580
Disease: Trichobezoar disorder
Trichobezoar disorder 		1 0 1 7.1E-02 0 0
CUI: C1834993
Disease: Prominent supraorbital arches in adult
Prominent supraorbital arches in adult 		1 0 1 7.1E-02 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 7.1E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 7.1E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 7.1E-02 0 0
CUI: C1837756
Disease: MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY 		1 0 1 7.1E-02 0 0
CUI: C1838779
Disease: Eiken Skeletal Dysplasia
Eiken Skeletal Dysplasia 		1 0 1 7.1E-02 0 0
CUI: C1839874
Disease: Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis 		1 0 1 7.1E-02 0 0