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: C0393524
Disease: Cerebellar Ataxia, Late Onset
Cerebellar Ataxia, Late Onset 		9 0 2 0.13 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 0.12 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 0.12 0 0
CUI: C0341266
Disease: Diverticulosis of the duodenum
Diverticulosis of the duodenum 		1 1 1 0.12 1 0.50
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 0.12 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 0.12 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 0.12 0 0
CUI: C0851121
Disease: digestive problem
digestive problem 		1 0 1 0.12 0 0
CUI: C1536114
Disease: Central pain syndrome
Central pain syndrome 		1 0 1 0.12 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 0.12 0 0
CUI: C1839785
Disease: Folate-dependent fragile site at Xq28
Folate-dependent fragile site at Xq28 		1 0 1 0.12 0 0
CUI: C3264595
Disease: Agoraphobia without panic disorder
Agoraphobia without panic disorder 		1 0 1 0.12 0 0
CUI: C3275367
Disease: Impaired tandem gait
Impaired tandem gait 		1 0 1 0.12 0 0
CUI: C3275521
Disease: CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME
CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME 		1 0 1 0.12 0 0
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 0.12 0 0
CUI: C3553947
Disease: PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER) 		1 0 1 0.12 0 0
CUI: C3553948
Disease: PEROXISOME BIOGENESIS DISORDER 6B
PEROXISOME BIOGENESIS DISORDER 6B 		1 0 1 0.12 0 0
CUI: C4016713
Disease: EPISODIC ATAXIA, TYPE 2, AND EPILEPSY
EPISODIC ATAXIA, TYPE 2, AND EPILEPSY 		1 0 1 0.12 0 0
CUI: C4021571
Disease: Abnormal vestibulo-ocular reflex
Abnormal vestibulo-ocular reflex 		1 0 1 0.12 0 0
CUI: C4024650
Disease: Congenital macroorchidism
Congenital macroorchidism 		1 0 1 0.12 0 0
CUI: C4310716
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42 		1 0 1 0.12 0 0
CUI: C4310787
Disease: CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION
CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION 		1 0 1 0.12 0 0
CUI: C4476868
Disease: Palpebral thickening
Palpebral thickening 		1 0 1 0.12 0 0
CUI: C4479246
Disease: CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER
CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER 		1 8 1 0.12 1 0.11
CUI: C0476236
Disease: Developmental symptoms
Developmental symptoms 		2 0 1 0.11 0 0