Source: INFERRED ×
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: C0855197
Disease: Malignant Testicular Germ Cell Tumor
Malignant Testicular Germ Cell Tumor 		0 50 0 0 1 1.7E-03
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		271 0 1 2.6E-03 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		242 0 1 2.8E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 2.9E-03 0 0
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 0 1 2.9E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 2.9E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		211 0 1 3.0E-03 0 0
CUI: C0085636
Disease: Photophobia
Photophobia 		210 0 1 3.0E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 3.1E-03 0 0
CUI: C0476273
Disease: Respiratory distress
Respiratory distress 		184 0 1 3.3E-03 0 0
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases 		179 0 1 3.4E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 3.4E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 3.5E-03 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		165 379 1 3.5E-03 1 1.1E-03
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 3.5E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 3.6E-03 0 0
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		161 0 1 3.6E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		157 0 1 3.6E-03 0 0
CUI: C0302511
Disease: Small for gestational age fetus
Small for gestational age fetus 		156 0 1 3.6E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		154 0 1 3.7E-03 0 0
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia 		153 0 1 3.7E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		150 0 1 3.7E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		146 0 1 3.8E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow 		141 0 1 3.9E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		136 0 1 3.9E-03 0 0