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: C4748555
Disease: MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE 		1 0 1 0.17 0 0
CUI: C2751544
Disease: BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 1
BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 1 		3 0 1 0.12 0 0
CUI: C4747394
Disease: CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 1
CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 1 		3 0 1 0.12 0 0
CUI: C0014740
Disease: Erythema Chronicum Migrans
Erythema Chronicum Migrans 		41 0 5 0.12 0 0
CUI: C0152417
Disease: Congenital stenosis of aortic valve
Congenital stenosis of aortic valve 		5 0 1 1.0E-01 0 0
CUI: C1864356
Disease: ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE
ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE 		5 0 1 1.0E-01 0 0
CUI: C2930970
Disease: Acromesomelic dysplasia Hunter-Thompson type
Acromesomelic dysplasia Hunter-Thompson type 		5 0 1 1.0E-01 0 0
CUI: C3838465
Disease: BASAL CELL CARCINOMA, SOMATIC
BASAL CELL CARCINOMA, SOMATIC 		5 0 1 1.0E-01 0 0
CUI: C0017677
Disease: Glossitis, Benign Migratory
Glossitis, Benign Migratory 		53 0 5 9.3E-02 0 0
CUI: C0242381
Disease: Lyme Arthritis
Lyme Arthritis 		57 0 5 8.6E-02 0 0
CUI: C0155567
Disease: Rheumatic aortic stenosis
Rheumatic aortic stenosis 		7 0 1 8.3E-02 0 0
CUI: C0333205
Disease: Mural thrombus
Mural thrombus 		7 0 1 8.3E-02 0 0
CUI: C1260883
Disease: Mural thrombus of heart
Mural thrombus of heart 		7 0 1 8.3E-02 0 0
CUI: C0085700
Disease: Chondromalacia
Chondromalacia 		8 0 1 7.7E-02 0 0
CUI: C4551627
Disease: Granulocytopenic disorder
Granulocytopenic disorder 		10 0 1 6.7E-02 0 0
CUI: C0679395
Disease: vascular ischemia
vascular ischemia 		12 0 1 5.9E-02 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis 		14 0 1 5.3E-02 0 0
CUI: C2931196
Disease: Craniofacial dysostosis type 1
Craniofacial dysostosis type 1 		15 0 1 5.0E-02 0 0
CUI: C0035086
Disease: Renal Osteodystrophy
Renal Osteodystrophy 		16 0 1 4.8E-02 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		16 0 1 4.8E-02 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 0 1 4.0E-02 0 0
CUI: C0267176
Disease: Gastroparesis with diabetes mellitus
Gastroparesis with diabetes mellitus 		21 0 1 3.8E-02 0 0
CUI: C1842180
Disease: CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)
CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder) 		22 0 1 3.7E-02 0 0
CUI: C0007302
Disease: Cartilage Diseases
Cartilage Diseases 		23 0 1 3.6E-02 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		28 0 1 3.0E-02 0 0