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: C0015544
Disease: Failure to Thrive
Failure to Thrive 		842 0 2 2.4E-03 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence 		60 0 2 3.3E-02 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		285 0 2 7.0E-03 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		446 0 1 2.2E-03 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma 		770 0 1 1.3E-03 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 0 1 1.3E-03 0 0
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		1760 0 1 5.7E-04 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		384 0 2 5.2E-03 0 0
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		1449 0 1 6.9E-04 0 0
CUI: C0019348
Disease: Herpes Simplex Infections
Herpes Simplex Infections 		645 0 1 1.5E-03 0 0
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		1098 0 1 9.1E-04 0 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		613 0 2 3.3E-03 0 0
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		1180 0 1 8.5E-04 0 0
CUI: C0023221
Disease: Leg Length Inequality
Leg Length Inequality 		27 0 2 7.4E-02 0 0
CUI: C0023267
Disease: Fibroid Tumor
Fibroid Tumor 		413 0 1 2.4E-03 0 0
CUI: C0023418
Disease: leukemia
leukemia 		2111 0 1 4.7E-04 0 0
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		1447 0 1 6.9E-04 0 0
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		1293 0 1 7.7E-04 0 0
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		1096 0 1 9.1E-04 0 0
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		3111 0 1 3.2E-04 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia 		148 0 2 1.4E-02 0 0
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		3806 0 1 2.6E-04 0 0
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		89 0 1 1.1E-02 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		505 0 1 2.0E-03 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly 		1064 0 1 9.4E-04 0 0