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: C0004048
Disease: Inspiration function
Inspiration function 		1 0 1 3.7E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 3.7E-02 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 3.7E-02 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 3.7E-02 0 0
CUI: C0267581
Disease: Rectal Stenosis
Rectal Stenosis 		1 0 1 3.7E-02 0 0
CUI: C0268486
Disease: Hereditary hypertyrosinemia
Hereditary hypertyrosinemia 		1 0 1 3.7E-02 0 0
CUI: C0344923
Disease: Multiple ventricular septal defects
Multiple ventricular septal defects 		1 0 1 3.7E-02 0 0
CUI: C0345286
Disease: Abnormal liver lobulation
Abnormal liver lobulation 		1 0 1 3.7E-02 0 0
CUI: C0495640
Disease: Congenital malformation syndromes involving early overgrowth
Congenital malformation syndromes involving early overgrowth 		1 0 1 3.7E-02 0 0
CUI: C0677861
Disease: Bilateral Malignant Neoplasm
Bilateral Malignant Neoplasm 		1 1 1 3.7E-02 1 0.50
CUI: C0859055
Disease: Oedema vascular
Oedema vascular 		1 0 1 3.7E-02 0 0
CUI: C1274594
Disease: Lichenoid actinic keratosis
Lichenoid actinic keratosis 		1 0 1 3.7E-02 0 0
CUI: C1275417
Disease: Non-involuting congenital hemangioma
Non-involuting congenital hemangioma 		1 0 1 3.7E-02 0 0
CUI: C1334664
Disease: Mediastinal Lymphangioma
Mediastinal Lymphangioma 		1 0 1 3.7E-02 0 0
CUI: C1335389
Disease: Lipomatosis of Nerve
Lipomatosis of Nerve 		1 0 1 3.7E-02 0 0
CUI: C1833508
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET 		1 0 1 3.7E-02 0 0
CUI: C1833511
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE 		1 0 1 3.7E-02 0 0
CUI: C1833518
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL 		1 0 1 3.7E-02 0 0
CUI: C1833541
Disease: Caroli disease isolated
Caroli disease isolated 		1 0 1 3.7E-02 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		1 0 1 3.7E-02 0 0
CUI: C1837273
Disease: Long-chain dicarboxylic aciduria
Long-chain dicarboxylic aciduria 		1 0 1 3.7E-02 0 0
CUI: C1842691
Disease: Diaphanospondylodysostosis
Diaphanospondylodysostosis 		1 0 1 3.7E-02 0 0
CUI: C1842695
Disease: Absent in utero rib ossification
Absent in utero rib ossification 		1 0 1 3.7E-02 0 0
CUI: C1842698
Disease: Absent in utero ossification of vertebral bodies
Absent in utero ossification of vertebral bodies 		1 0 1 3.7E-02 0 0
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 3.7E-02 0 0