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: C0345963
Disease: Benign neoplasm of lung
Benign neoplasm of lung 		0 1 0 0 1 1.0E-01
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 0.20
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 0.20
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 2.0E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 2.1E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.3E-03 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		168 0 1 2.3E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 2.3E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		135 0 1 2.5E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.5E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 2.5E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.5E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 2.6E-03 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 0 1 2.6E-03 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 1 2.6E-03 0 0
CUI: C0020458
Disease: Hyperhidrosis disorder
Hyperhidrosis disorder 		114 0 1 2.6E-03 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder) 		109 0 1 2.6E-03 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 1 2.6E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		105 0 1 2.6E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 2.7E-03 0 0
CUI: C0282577
Disease: Congenital Disorders of Glycosylation
Congenital Disorders of Glycosylation 		102 0 1 2.7E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 1 2.7E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation 		98 0 1 2.7E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 2.7E-03 0 0
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border 		95 0 1 2.7E-03 0 0