Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Autosomal dominant spondylocostal dysostosis
3 0 2 1.0E-01 0 0
CUI: C0265695
Disease: Congenital fusion of ribs
Congenital fusion of ribs
37 0 5 9.8E-02 0 0
CUI: C0266345
Disease: Congenital urethral valve
Congenital urethral valve
5 0 2 9.1E-02 0 0
Short distal phalanx of the 5th finger
6 0 2 8.7E-02 0 0
CUI: C1851720
Disease: Adrenocortical cytomegaly
Adrenocortical cytomegaly
6 0 2 8.7E-02 0 0
CUI: C1851722
Disease: Overgrowth of external genitalia
Overgrowth of external genitalia
6 0 2 8.7E-02 0 0
CUI: C1851733
Disease: Pancreatic hyperplasia
Pancreatic hyperplasia
6 0 2 8.7E-02 0 0
CUI: C4023014
Disease: Stereotypical hand wringing
Stereotypical hand wringing
8 0 2 8.0E-02 0 0
CUI: C0265677
Disease: Congenital hemivertebra
Congenital hemivertebra
49 0 5 7.9E-02 0 0
CUI: C0221766
Disease: Diastasis recti
Diastasis recti
22 0 3 7.9E-02 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead
133 0 11 7.8E-02 0 0
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy
23 0 3 7.7E-02 0 0
CUI: C0426789
Disease: Short thorax
Short thorax
51 0 5 7.7E-02 0 0
CUI: C1867114
Disease: Craniofacial disproportion
Craniofacial disproportion
9 0 2 7.7E-02 0 0
CUI: C4021539
Disease: Posterior helix pit
Posterior helix pit
9 0 2 7.7E-02 0 0
CUI: C1860245
Disease: Cranial asymmetry
Cranial asymmetry
10 0 2 7.4E-02 0 0
CUI: C0266039
Disease: Taurodontism
Taurodontism
40 0 4 7.3E-02 0 0
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney
40 0 4 7.3E-02 0 0
CUI: C4021777
Disease: Abnormality of the larynx
Abnormality of the larynx
11 0 2 7.1E-02 0 0
CUI: C1858033
Disease: Asymmetry of the thorax
Asymmetry of the thorax
12 0 2 6.9E-02 0 0
CUI: C4744565
Disease: Metastatic Colon Carcinoma
Metastatic Colon Carcinoma
12 0 2 6.9E-02 0 0
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
59 0 5 6.8E-02 0 0
CUI: C0347284
Disease: Benign tumor of pancreas
Benign tumor of pancreas
13 0 2 6.7E-02 0 0
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines
13 0 2 6.7E-02 0 0
CUI: C0022739
Disease: Klippel-Trenaunay-Weber Syndrome
Klippel-Trenaunay-Weber Syndrome
14 0 2 6.5E-02 0 0