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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		0 11 0 0 1 1.6E-04
CUI: C0206064
Disease: Microvascular Angina
Microvascular Angina 		0 10 0 0 2 3.1E-04
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 2 3.1E-04
CUI: C0345906
Disease: Sarcoma of liver
Sarcoma of liver 		0 1 0 0 1 1.6E-04
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait 		0 2 0 0 1 1.6E-04
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 1.6E-04
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 1.6E-04
CUI: C1969144
Disease: Renal cortical cysts
Renal cortical cysts 		0 1 0 0 1 1.6E-04
CUI: C3887608
Disease: HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1 		0 6 0 0 1 1.6E-04
CUI: C4225180
Disease: EVEN-PLUS SYNDROME
EVEN-PLUS SYNDROME 		0 5 0 0 1 1.6E-04
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 1 1.5E-03 0 0
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		399 0 1 2.1E-03 0 0
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		336 0 1 2.4E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 1 2.5E-03 0 0
CUI: C0027059
Disease: Myocarditis
Myocarditis 		285 0 1 2.7E-03 0 0
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		656 0 2 2.7E-03 0 0
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		280 0 1 2.7E-03 0 0
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior 		276 0 1 2.8E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.8E-03 0 0
CUI: C0476273
Disease: Respiratory distress
Respiratory distress 		259 0 1 2.9E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 3.1E-03 0 0
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		234 0 1 3.1E-03 0 0
CUI: C0004610
Disease: Bacteremia
Bacteremia 		233 0 1 3.1E-03 0 0
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 0 1 3.2E-03 0 0
CUI: C0085636
Disease: Photophobia
Photophobia 		227 0 1 3.2E-03 0 0