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: C0268181
Disease: Lactose Intolerance, Adult Type
Lactose Intolerance, Adult Type 		7 0 4 0.29 0 0
CUI: C4476604
Disease: Decreased small intestinal mucosa lactase activity
Decreased small intestinal mucosa lactase activity 		2 0 2 0.18 0 0
CUI: C0006705
Disease: Calcium Metabolism Disorders
Calcium Metabolism Disorders 		5 0 2 0.14 0 0
CUI: C1857231
Disease: LACTASE PERSISTENCE
LACTASE PERSISTENCE 		15 0 3 0.13 0 0
CUI: C1855841
Disease: Hypocalcemic seizures
Hypocalcemic seizures 		11 0 2 1.0E-01 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 9.1E-02 0 0
CUI: C0162677
Disease: Caliciviridae Infections
Caliciviridae Infections 		1 0 1 9.1E-02 0 0
CUI: C0268179
Disease: Lactase Deficiency, Congenital
Lactase Deficiency, Congenital 		1 0 1 9.1E-02 0 0
CUI: C0343379
Disease: Enterotoxigenic Escherichia coli gastrointestinal tract infection
Enterotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 9.1E-02 0 0
CUI: C0477611
Disease: [X]Spinal osteochondrosis, unspecified
[X]Spinal osteochondrosis, unspecified 		1 0 1 9.1E-02 0 0
CUI: C0521527
Disease: Shortened trunk
Shortened trunk 		1 0 1 9.1E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 9.1E-02 0 0
CUI: C0856247
Disease: Lumbar spine degeneration
Lumbar spine degeneration 		1 0 1 9.1E-02 0 0
CUI: C0860471
Disease: Dairy intolerance
Dairy intolerance 		1 0 1 9.1E-02 0 0
CUI: C0860475
Disease: Lactose intolerant
Lactose intolerant 		1 0 1 9.1E-02 0 0
CUI: C0948755
Disease: Pulmonary failure
Pulmonary failure 		1 0 1 9.1E-02 0 0
CUI: C1321580
Disease: Trichobezoar disorder
Trichobezoar disorder 		1 0 1 9.1E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 9.1E-02 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 9.1E-02 0 0
CUI: C1848795
Disease: GRAVES DISEASE, SUSCEPTIBILITY TO, 1
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 		1 1 1 9.1E-02 1 0.50
CUI: C1857692
Disease: Venous varicosities of celiac and mesenteric vessels
Venous varicosities of celiac and mesenteric vessels 		1 0 1 9.1E-02 0 0
CUI: C1968633
Disease: Intimal thickening in the coronary arteries
Intimal thickening in the coronary arteries 		1 0 1 9.1E-02 0 0
CUI: C1968748
Disease: Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement
Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement 		1 0 1 9.1E-02 0 0
CUI: C2674252
Disease: VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1
VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1 		1 0 1 9.1E-02 0 0
CUI: C2752062
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8 		1 0 1 9.1E-02 0 0