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: C0403819
Disease: Acquired obstructive azoospermia
Acquired obstructive azoospermia 		1 0 1 5.3E-02 0 0
CUI: C0406425
Disease: Laugier-Hunziker syndrome
Laugier-Hunziker syndrome 		1 0 1 5.3E-02 0 0
CUI: C0406814
Disease: Labial lentigo
Labial lentigo 		1 0 1 5.3E-02 0 0
CUI: C0456487
Disease: Peutz Jehgers polyp
Peutz Jehgers polyp 		1 0 1 5.3E-02 0 0
CUI: C0496924
Disease: Neoplasm of uncertain or unknown behavior of testis
Neoplasm of uncertain or unknown behavior of testis 		1 0 1 5.3E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 5.3E-02 0 0
CUI: C0740266
Disease: Anal and rectal conditions
Anal and rectal conditions 		1 0 1 5.3E-02 0 0
CUI: C0854110
Disease: Insulin-resistant diabetes mellitus
Insulin-resistant diabetes mellitus 		21 0 2 5.3E-02 0 0
CUI: C0860006
Disease: Hypotonic dehydration
Hypotonic dehydration 		1 0 1 5.3E-02 0 0
CUI: C0877664
Disease: Gastrointestinal cramps
Gastrointestinal cramps 		1 0 1 5.3E-02 0 0
CUI: C0948783
Disease: Bronchopulmonary infection
Bronchopulmonary infection 		1 0 1 5.3E-02 0 0
CUI: C1142307
Disease: Paratubal Cyst
Paratubal Cyst 		1 0 1 5.3E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 5.3E-02 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF 		1 0 1 5.3E-02 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF 		1 0 1 5.3E-02 0 0
CUI: C1832253
Disease: INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF 		1 0 1 5.3E-02 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 5.3E-02 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1 		1 0 1 5.3E-02 0 0
CUI: C1837991
Disease: Colorectal Adenomatous Polyposis, Autosomal Recessive
Colorectal Adenomatous Polyposis, Autosomal Recessive 		1 0 1 5.3E-02 0 0
CUI: C1865433
Disease: VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF
VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF 		1 0 1 5.3E-02 0 0
CUI: C1865553
Disease: HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO
HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 5.3E-02 0 0
CUI: C1868007
Disease: Precocious puberty with Sertoli cell tumor
Precocious puberty with Sertoli cell tumor 		1 0 1 5.3E-02 0 0
CUI: C1963822
Disease: Mucosal pigmentation
Mucosal pigmentation 		1 0 1 5.3E-02 0 0
CUI: C2752062
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8 		1 0 1 5.3E-02 0 0
CUI: C4016735
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF 		1 0 1 5.3E-02 0 0