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: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		0 1 0 0 1 7.1E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 7.1E-03
CUI: C2750733
Disease: LEPROSY, SUSCEPTIBILITY TO, 5
LEPROSY, SUSCEPTIBILITY TO, 5 		0 1 0 0 1 7.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 3 2.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 7.1E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 2.1E-02
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 1 8.1E-04 0 0
CUI: C0406208
Disease: Suntan
Suntan 		53 0 1 8.1E-04 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate 		45 0 1 8.2E-04 0 0
CUI: C4551906
Disease: Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		43 0 1 8.2E-04 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 8.2E-04 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		41 0 1 8.2E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 8.2E-04 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 8.2E-04 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity 		41 0 1 8.2E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 8.2E-04 0 0
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 1 8.2E-04 0 0
CUI: C4021608
Disease: Shortening of all distal phalanges of the fingers
Shortening of all distal phalanges of the fingers 		40 0 1 8.2E-04 0 0
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder 		39 0 1 8.2E-04 0 0
CUI: C1847515
Disease: Paroxysmal involuntary eye movements
Paroxysmal involuntary eye movements 		39 0 1 8.2E-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 8.2E-04 0 0
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly 		36 0 1 8.2E-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 8.2E-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 8.2E-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 8.2E-04 0 0