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: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
512 0 1 1.9E-03 0 0
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
560 0 1 1.8E-03 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
842 0 1 1.2E-03 0 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
523 0 1 1.9E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 1 1.7E-03 0 0
CUI: C0026848
Disease: Myopathy
Myopathy
634 0 1 1.6E-03 0 0
CUI: C0036572
Disease: Seizures
Seizures
2152 0 1 4.6E-04 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
144 0 1 6.9E-03 0 0
CUI: C0042963
Disease: Vomiting
Vomiting
303 0 1 3.3E-03 0 0
CUI: C0085584
Disease: Encephalopathies
Encephalopathies
457 0 1 2.2E-03 0 0
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
536 0 1 1.9E-03 0 0
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
121 0 1 8.2E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 0 1 2.1E-03 0 0
CUI: C0234133
Disease: Extrapyramidal sign
Extrapyramidal sign
116 0 1 8.5E-03 0 0
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia
14 0 1 6.7E-02 0 0
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
189 0 1 5.3E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation
98 0 1 1.0E-02 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
187 0 1 5.3E-03 0 0
CUI: C0747251
Disease: Progressive spastic paraparesis
Progressive spastic paraparesis
14 0 1 6.7E-02 0 0
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
284 0 1 3.5E-03 0 0
CUI: C0751748
Disease: Nonketotic Hyperglycinemia
Nonketotic Hyperglycinemia
21 0 1 4.5E-02 0 0
CUI: C0751783
Disease: Lafora Disease
Lafora Disease
92 0 1 1.1E-02 0 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
925 0 1 1.1E-03 0 0
CUI: C1305855
Disease: Body mass index
Body mass index
1014 0 1 9.9E-04 0 0
CUI: C1836038
Disease: Poor head control
Poor head control
162 0 1 6.1E-03 0 0