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: C0919677
Disease: Protein C measurement
Protein C measurement 		62 0 1 5.6E-04 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		62 0 1 5.6E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 5.6E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 5.7E-04 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 5.7E-04 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 5.7E-04 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition 		40 0 1 5.7E-04 0 0
CUI: C1838951
Disease: LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 1 5.7E-04 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		39 0 1 5.7E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 5.7E-04 0 0
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy 		38 0 1 5.7E-04 0 0
CUI: C1850599
Disease: Leigh Syndrome due to Mitochondrial Complex IV Deficiency
Leigh Syndrome due to Mitochondrial Complex IV Deficiency 		37 0 1 5.7E-04 0 0
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		36 0 1 5.7E-04 0 0
CUI: C1850598
Disease: Leigh Syndrome due to Mitochondrial Complex III Deficiency
Leigh Syndrome due to Mitochondrial Complex III Deficiency 		36 0 1 5.7E-04 0 0
CUI: C1850600
Disease: Leigh Syndrome due to Mitochondrial Complex V Deficiency
Leigh Syndrome due to Mitochondrial Complex V Deficiency 		36 0 1 5.7E-04 0 0
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		36 0 1 5.7E-04 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 1 5.7E-04 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 1 5.7E-04 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		35 0 1 5.7E-04 0 0
CUI: C4553976
Disease: Urinary Urgency, CTCAE 5
Urinary Urgency, CTCAE 5 		34 0 1 5.7E-04 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		33 0 1 5.7E-04 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 0 1 5.7E-04 0 0
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination 		32 0 1 5.7E-04 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness 		31 0 1 5.7E-04 0 0
CUI: C0038663
Disease: Suicide attempt
Suicide attempt 		31 0 1 5.7E-04 0 0