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: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 1 9.1E-04 0 0
CUI: C0003578
Disease: Apnea
Apnea 		262 0 1 3.8E-03 0 0
CUI: C0004509
Disease: Azoospermia
Azoospermia 		254 0 1 3.9E-03 0 0
CUI: C0006266
Disease: Bronchospasm
Bronchospasm 		29 0 1 3.4E-02 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		725 0 1 1.4E-03 0 0
CUI: C0011570
Disease: Mental Depression
Mental Depression 		1478 0 1 6.8E-04 0 0
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		1719 0 1 5.8E-04 0 0
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		148 0 1 6.8E-03 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		446 0 1 2.2E-03 0 0
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest 		411 0 1 2.4E-03 0 0
CUI: C0020672
Disease: Hypothermia, natural
Hypothermia, natural 		52 0 1 1.9E-02 0 0
CUI: C0021364
Disease: Male infertility
Male infertility 		516 0 1 1.9E-03 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm 		48 0 1 2.1E-02 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus 		265 0 1 3.8E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 4.6E-03 0 0
CUI: C0036875
Disease: Disorders of Sex Development
Disorders of Sex Development 		39 0 1 2.6E-02 0 0
CUI: C0037315
Disease: Sleep Apnea Syndromes
Sleep Apnea Syndromes 		148 0 1 6.8E-03 0 0
CUI: C0038450
Disease: Stridor
Stridor 		31 0 1 3.2E-02 0 0
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		140 0 1 7.1E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 1 3.2E-03 0 0
CUI: C0239548
Disease: Fasciculation, Tongue
Fasciculation, Tongue 		21 0 1 4.8E-02 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		109 0 1 9.2E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 4.2E-03 0 0
CUI: C0271994
Disease: Hereditary persistence of fetal hemoglobin thalassemia
Hereditary persistence of fetal hemoglobin thalassemia 		35 0 1 2.9E-02 0 0
CUI: C0302885
Disease: Testicular dysgenesis
Testicular dysgenesis 		13 0 1 7.7E-02 0 0