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: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 4.3E-02
CUI: C4524071
Disease: Philadelphia positive acute lymphocytic leukaemia
Philadelphia positive acute lymphocytic leukaemia 		0 1 0 0 1 4.3E-02
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 1.6E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation 		98 0 1 1.7E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls 		94 0 1 1.8E-03 0 0
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		89 0 1 1.8E-03 0 0
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		89 0 1 1.8E-03 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 1 1.8E-03 0 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		80 0 1 1.8E-03 0 0
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		80 0 1 1.8E-03 0 0
CUI: C0015310
Disease: Exotropia
Exotropia 		78 0 1 1.8E-03 0 0
CUI: C0456132
Disease: Large fontanelle
Large fontanelle 		77 0 1 1.8E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		75 0 1 1.8E-03 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 1 1.8E-03 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		71 0 1 1.8E-03 0 0
CUI: C1842083
Disease: Abnormality of the ribs
Abnormality of the ribs 		69 0 1 1.8E-03 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 0 1 1.8E-03 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		66 0 1 1.8E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 1.8E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 1.8E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 1.9E-03 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		62 0 1 1.9E-03 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		62 0 1 1.9E-03 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		61 0 1 1.9E-03 0 0
CUI: C0162283
Disease: Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus 		60 0 1 1.9E-03 0 0