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: C0266432
Disease: Leydig cell agenesis
Leydig cell agenesis 		0 21 0 0 1 2.4E-02
CUI: C0949083
Disease: Hospital acquired pneumonia
Hospital acquired pneumonia 		0 2 0 0 1 4.5E-02
CUI: C1443237
Disease: Healthcare associated pneumonia
Healthcare associated pneumonia 		0 2 0 0 1 4.5E-02
CUI: C2673497
Disease: Leydig Cell Hypoplasia, Type II
Leydig Cell Hypoplasia, Type II 		0 2 0 0 1 4.5E-02
CUI: C4022708
Disease: Midshaft hypospadias
Midshaft hypospadias 		0 1 0 0 1 4.8E-02
CUI: C0016724
Disease: Froehlich's Syndrome
Froehlich's Syndrome 		1 0 1 3.1E-02 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male 		1 0 1 3.1E-02 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 3.1E-02 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 3.1E-02 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 3.1E-02 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 3.1E-02 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 3.1E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 3.1E-02 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 3.1E-02 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia 		1 0 1 3.1E-02 0 0
CUI: C0236099
Disease: Disorder of male reproductive system
Disorder of male reproductive system 		1 0 1 3.1E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 3.1E-02 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 3.1E-02 0 0
CUI: C0264487
Disease: Chronic nonspecific lung disease
Chronic nonspecific lung disease 		1 0 1 3.1E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 3.1E-02 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 3.1E-02 0 0
CUI: C0266430
Disease: Polyorchism
Polyorchism 		1 0 1 3.1E-02 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 3.1E-02 0 0
CUI: C0339678
Disease: Simple myopia
Simple myopia 		1 0 1 3.1E-02 0 0
CUI: C0342134
Disease: T>3< thyrotoxicosis
T>3< thyrotoxicosis 		1 0 1 3.1E-02 0 0