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: C0043379
Disease: XYY Karyotype
XYY Karyotype 		1 0 1 1.6E-02 0 0
CUI: C0265756
Disease: Congenital atresia of larynx
Congenital atresia of larynx 		1 0 1 1.6E-02 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 1.6E-02 0 0
CUI: C0270629
Disease: Epidural Abscess
Epidural Abscess 		1 0 1 1.6E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 1.6E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 1.6E-02 0 0
CUI: C0342278
Disease: Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 		1 0 1 1.6E-02 0 0
CUI: C0431289
Disease: Frontal Encephalocele
Frontal Encephalocele 		1 0 1 1.6E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 1.6E-02 0 0
CUI: C0432361
Disease: Diffuse neurofibroma
Diffuse neurofibroma 		1 0 1 1.6E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 1.6E-02 0 0
CUI: C0796046
Disease: Gurrieri Sammito Bellussi syndrome
Gurrieri Sammito Bellussi syndrome 		1 0 1 1.6E-02 0 0
CUI: C0878515
Disease: Internal hydrocephalus
Internal hydrocephalus 		1 0 1 1.6E-02 0 0
CUI: C1280777
Disease: displaced uterus
displaced uterus 		1 0 1 1.6E-02 0 0
CUI: C1291329
Disease: Transaldolase Deficiency
Transaldolase Deficiency 		1 0 1 1.6E-02 0 0
CUI: C1319016
Disease: Nephrogenic rest, intralobar
Nephrogenic rest, intralobar 		1 0 1 1.6E-02 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma 		1 0 1 1.6E-02 0 0
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 1.6E-02 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 1.6E-02 0 0
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		1 0 1 1.6E-02 0 0
CUI: C1837530
Disease: AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency 		1 0 1 1.6E-02 0 0
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		1 0 1 1.6E-02 0 0
CUI: C1849185
Disease: Elevated 7-dehydrocholesterol
Elevated 7-dehydrocholesterol 		1 0 1 1.6E-02 0 0
CUI: C1849316
Disease: Premature separation of centromeric heterochromatin
Premature separation of centromeric heterochromatin 		1 0 1 1.6E-02 0 0
CUI: C1849370
Disease: Tetraphocomelia
Tetraphocomelia 		1 0 1 1.6E-02 0 0