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: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.1E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		264 0 1 2.1E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.6E-03 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		168 0 1 2.6E-03 0 0
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		166 122 1 2.6E-03 1 7.9E-03
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 2.6E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.7E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 2.7E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 2.8E-03 0 0
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		145 0 1 2.8E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial 		142 0 1 2.8E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 1 2.8E-03 0 0
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		135 0 1 2.9E-03 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 0 1 2.9E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		124 0 1 2.9E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 3.0E-03 0 0
CUI: C0039070
Disease: Syncope
Syncope 		119 0 1 3.0E-03 0 0
CUI: C0476254
Disease: Dyslexia
Dyslexia 		118 0 1 3.0E-03 0 0
CUI: C3811918
Disease: GRN-related frontotemporal dementia
GRN-related frontotemporal dementia 		112 0 1 3.1E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 3.1E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		105 0 1 3.1E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 3.1E-03 0 0
CUI: C0282577
Disease: Congenital Disorders of Glycosylation
Congenital Disorders of Glycosylation 		102 0 1 3.2E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 1 3.2E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 3.2E-03 0 0