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: C0027854
Disease: Neurologic Manifestations
Neurologic Manifestations 		12 0 1 7.1E-02 0 0
CUI: C0701818
Disease: Choledocholithiasis
Choledocholithiasis 		12 0 1 7.1E-02 0 0
CUI: C1266708
Disease: Polybrominated biphenyl measurement
Polybrominated biphenyl measurement 		12 0 1 7.1E-02 0 0
CUI: C0750905
Disease: Amino Acid Metabolism, Inherited Disorders
Amino Acid Metabolism, Inherited Disorders 		13 0 1 6.7E-02 0 0
CUI: C0007398
Disease: Catatonia
Catatonia 		14 0 1 6.2E-02 0 0
CUI: C0543541
Disease: HYPERGLYCINURIA (disorder)
HYPERGLYCINURIA (disorder) 		14 0 1 6.2E-02 0 0
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		53 92 3 5.7E-02 3 3.3E-02
CUI: C1332884
Disease: Central nervous system leukaemia
Central nervous system leukaemia 		17 0 1 5.3E-02 0 0
CUI: C0020617
Disease: Hypoglycemic coma
Hypoglycemic coma 		19 0 1 4.8E-02 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 4.5E-02 0 0
CUI: C4225412
Disease: Spondylo-ocular syndrome
Spondylo-ocular syndrome 		24 0 1 3.8E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		31 0 1 3.0E-02 0 0
CUI: C1955906
Disease: Lymphoma, Extranodal NK-T-Cell
Lymphoma, Extranodal NK-T-Cell 		33 0 1 2.9E-02 0 0
CUI: C0019156
Disease: Hepatic Veno-Occlusive Disease
Hepatic Veno-Occlusive Disease 		37 0 1 2.6E-02 0 0
CUI: C2986717
Disease: Anti-N-Methyl-D-Aspartate Receptor Encephalitis
Anti-N-Methyl-D-Aspartate Receptor Encephalitis 		43 0 1 2.2E-02 0 0
CUI: C4721444
Disease: Burkitt Leukemia
Burkitt Leukemia 		45 0 1 2.1E-02 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		46 0 1 2.1E-02 0 0
CUI: C0920028
Disease: Leukaemia recurrent
Leukaemia recurrent 		50 0 1 1.9E-02 0 0
CUI: C1855496
Disease: Contiguous gene syndrome
Contiguous gene syndrome 		52 0 1 1.9E-02 0 0
CUI: C0392788
Disease: Nasal Type Extranodal NK/T-Cell Lymphoma
Nasal Type Extranodal NK/T-Cell Lymphoma 		53 0 1 1.8E-02 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis 		55 0 1 1.8E-02 0 0
CUI: C4316812
Disease: Fibrinogen Deficiency
Fibrinogen Deficiency 		56 0 1 1.7E-02 0 0
CUI: C1302790
Disease: Congenital malformation syndrome
Congenital malformation syndrome 		57 0 1 1.7E-02 0 0
CUI: C0024591
Disease: Malignant hyperpyrexia due to anesthesia
Malignant hyperpyrexia due to anesthesia 		60 0 1 1.6E-02 0 0
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia 		60 0 1 1.6E-02 0 0