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: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 1 9.1E-04 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 4.0E-03 0 0
Congenital arteriovenous malformation
163 0 1 6.1E-03 0 0
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
2723 0 1 3.7E-04 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 1 1.2E-03 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
1112 0 1 9.0E-04 0 0
CUI: C0005747
Disease: Blepharospasm
Blepharospasm
44 0 1 2.3E-02 0 0
CUI: C0006111
Disease: Brain Diseases
Brain Diseases
345 0 1 2.9E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
441 0 1 2.3E-03 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities
355 0 1 2.8E-03 0 0
Child Development Disorders, Pervasive
168 0 1 6.0E-03 0 0
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders
607 0 1 1.6E-03 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism
1261 0 1 7.9E-04 0 0
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome
316 0 1 3.2E-03 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy
1215 0 1 8.2E-04 0 0
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized
93 0 1 1.1E-02 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy
71 0 1 1.4E-02 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
842 0 1 1.2E-03 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
446 0 1 2.2E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia
218 0 1 4.6E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 1 6.3E-03 0 0
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
276 0 1 3.6E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders
94 0 1 1.1E-02 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial
142 0 1 7.0E-03 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
1064 0 1 9.4E-04 0 0