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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 1.1E-02 0 0
CUI: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 1.1E-02 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 1.1E-02 0 0
CUI: C0020683
Disease: Hypovolemic Shock
Hypovolemic Shock 		1 0 1 1.1E-02 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 1.1E-02 0 0
CUI: C0025060
Disease: Mediastinal Cyst
Mediastinal Cyst 		1 0 1 1.1E-02 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 1.1E-02 0 0
CUI: C0027656
Disease: Neoplasms, Connective Tissue
Neoplasms, Connective Tissue 		1 0 1 1.1E-02 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 1.1E-02 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 1.1E-02 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension 		1 0 1 1.1E-02 0 0
CUI: C0233525
Disease: Defensive aggression
Defensive aggression 		1 0 1 1.1E-02 0 0
CUI: C0238525
Disease: Sarcoma of vulva
Sarcoma of vulva 		1 0 1 1.1E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 1.1E-02 0 0
CUI: C0240583
Disease: Short upturned nose
Short upturned nose 		1 0 1 1.1E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 1.1E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 1.1E-02 0 0
CUI: C0265263
Disease: Femoral hypoplasia - unusual facies syndrome
Femoral hypoplasia - unusual facies syndrome 		1 0 1 1.1E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 1.1E-02 0 0
CUI: C0265756
Disease: Congenital atresia of larynx
Congenital atresia of larynx 		1 0 1 1.1E-02 0 0
CUI: C0265856
Disease: Hypoplasia of right heart
Hypoplasia of right heart 		1 0 1 1.1E-02 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 1.1E-02 0 0
CUI: C0266429
Disease: Monorchism
Monorchism 		1 0 1 1.1E-02 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 1.1E-02 0 0
CUI: C0268221
Disease: Fucosidosis Type I
Fucosidosis Type I 		1 0 1 1.1E-02 0 0