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: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy 		8 0 1 1.0E-01 0 0
CUI: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome 		8 0 1 1.0E-01 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 1 1.0E-01 0 0
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		20 0 2 9.5E-02 0 0
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		20 0 2 9.5E-02 0 0
CUI: C1963674
Disease: Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 10 		9 0 1 9.1E-02 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 1 8.3E-02 0 0
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 0 1 8.3E-02 0 0
CUI: C0023009
Disease: Speech and language disorder
Speech and language disorder 		11 0 1 7.7E-02 0 0
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal 		11 0 1 7.7E-02 0 0
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 0 1 7.1E-02 0 0
CUI: C0393519
Disease: Cerebellar Ataxia, Early Onset
Cerebellar Ataxia, Early Onset 		12 0 1 7.1E-02 0 0
CUI: C0428578
Disease: Iron level result
Iron level result 		12 0 1 7.1E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3 		12 0 1 7.1E-02 0 0
CUI: C1519787
Disease: Undifferentiated Neuroblastoma
Undifferentiated Neuroblastoma 		12 0 1 7.1E-02 0 0
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas 		13 0 1 6.7E-02 0 0
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration 		14 0 1 6.2E-02 0 0
CUI: C3276549
Disease: OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY 		14 0 1 6.2E-02 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 0 1 5.9E-02 0 0
CUI: C1849148
Disease: Decreased sensory nerve conduction velocity
Decreased sensory nerve conduction velocity 		15 0 1 5.9E-02 0 0
CUI: C1856691
Disease: Impaired proprioception
Impaired proprioception 		15 0 1 5.9E-02 0 0
CUI: C1866751
Disease: Spinocerebellar tract degeneration
Spinocerebellar tract degeneration 		15 0 1 5.9E-02 0 0
CUI: C0002884
Disease: Hypochromic anemia
Hypochromic anemia 		16 0 1 5.6E-02 0 0
CUI: C0154671
Disease: Degenerative brain disorder
Degenerative brain disorder 		16 0 1 5.6E-02 0 0
CUI: C0393556
Disease: Complicated hereditary spastic paraplegia
Complicated hereditary spastic paraplegia 		16 0 1 5.6E-02 0 0