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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.5E-03
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 0 0 1 3.5E-03
CUI: C0476482
Disease: Restlessness and agitation
Restlessness and agitation 		0 1 0 0 1 3.5E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 3.5E-03
CUI: C3150344
Disease: HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED
HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED 		0 24 0 0 1 3.2E-03
CUI: C3502110
Disease: Homocystinuria, Pyridoxine-Responsive
Homocystinuria, Pyridoxine-Responsive 		0 11 0 0 2 6.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.5E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.5E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 3.5E-03
CUI: C0013592
Disease: Ectropion
Ectropion 		50 0 1 9.1E-04 0 0
CUI: C0426818
Disease: Thin rib
Thin rib 		42 0 1 9.2E-04 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 1 9.2E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 9.2E-04 0 0
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		39 0 1 9.2E-04 0 0
CUI: C0472767
Disease: Beta thalassemia intermedia
Beta thalassemia intermedia 		37 0 1 9.2E-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 9.2E-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 9.2E-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 9.2E-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 9.2E-04 0 0
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		36 0 1 9.2E-04 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 1 9.2E-04 0 0
CUI: C0221365
Disease: Double ureter
Double ureter 		34 0 1 9.3E-04 0 0
CUI: C1314694
Disease: Astrocytoma, low grade
Astrocytoma, low grade 		34 0 1 9.3E-04 0 0
CUI: C0392163
Disease: Corneal erosion
Corneal erosion 		33 0 1 9.3E-04 0 0
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion 		33 0 1 9.3E-04 0 0