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 4.0E-02
CUI: C1290073
Disease: Acute mucositis
Acute mucositis 		0 1 0 0 1 4.0E-02
CUI: C4524071
Disease: Philadelphia positive acute lymphocytic leukaemia
Philadelphia positive acute lymphocytic leukaemia 		0 1 0 0 1 4.0E-02
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 8.6E-04 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 9.2E-04 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 1 9.4E-04 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 9.4E-04 0 0
CUI: C0009024
Disease: Clonus
Clonus 		60 0 1 9.5E-04 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 9.5E-04 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia 		59 0 1 9.5E-04 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		59 0 1 9.5E-04 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 9.5E-04 0 0
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		57 0 1 9.5E-04 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 1 9.5E-04 0 0
CUI: C0575059
Disease: Spastic tetraparesis
Spastic tetraparesis 		50 0 1 9.6E-04 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 9.6E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 9.6E-04 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus 		46 0 1 9.6E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 9.6E-04 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 9.6E-04 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 9.6E-04 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility 		45 0 1 9.6E-04 0 0
CUI: C1837402
Disease: Flat occiput
Flat occiput 		45 0 1 9.6E-04 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate 		45 0 1 9.6E-04 0 0
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		43 0 1 9.6E-04 0 0