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: C0000729
Disease: Abdominal Cramps
Abdominal Cramps 		1 0 1 6.5E-03 0 0
CUI: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 6.5E-03 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 6.5E-03 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst 		1 2 1 6.5E-03 2 7.7E-02
CUI: C0026684
Disease: Mucocele of appendix
Mucocele of appendix 		1 0 1 6.5E-03 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 6.5E-03 0 0
CUI: C0037932
Disease: Curvature of spine
Curvature of spine 		1 0 1 6.5E-03 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 1 1 6.5E-03 1 3.8E-02
CUI: C0155411
Disease: Exostosis of external ear canal
Exostosis of external ear canal 		1 0 1 6.5E-03 0 0
CUI: C0157733
Disease: Abnormality of the hair
Abnormality of the hair 		1 0 1 6.5E-03 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 6.5E-03 0 0
CUI: C0201896
Disease: Arylsulfatase B measurement
Arylsulfatase B measurement 		1 0 1 6.5E-03 0 0
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors 		1 2 1 6.5E-03 2 7.7E-02
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 6.5E-03 0 0
CUI: C0220743
Disease: Childhood hypophosphatasia (disorder)
Childhood hypophosphatasia (disorder) 		1 0 1 6.5E-03 0 0
CUI: C0234918
Disease: Morbilliform rash
Morbilliform rash 		1 0 1 6.5E-03 0 0
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 6.5E-03 0 0
CUI: C0240709
Disease: Pericardial constriction
Pericardial constriction 		1 0 1 6.5E-03 0 0
CUI: C0264954
Disease: Arteriovascular degeneration
Arteriovascular degeneration 		1 0 1 6.5E-03 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 6.5E-03 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 6.5E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 6.5E-03 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 6.5E-03 0 0
CUI: C0265809
Disease: Double outlet left ventricle
Double outlet left ventricle 		1 0 1 6.5E-03 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 6.5E-03 0 0