Source: CLINVAR ×
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: C0003706
Disease: Arachnodactyly
Arachnodactyly 		0 24 0 0 1 3.7E-03
CUI: C0014394
Disease: Enuresis
Enuresis 		0 3 0 0 1 4.0E-03
CUI: C0038220
Disease: Status Epilepticus
Status Epilepticus 		0 6 0 0 1 4.0E-03
CUI: C0241521
Disease: Ulnar deviation of hand
Ulnar deviation of hand 		0 2 0 0 1 4.0E-03
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		0 10 0 0 1 3.9E-03
CUI: C0850703
Disease: Frequent falls
Frequent falls 		0 4 0 0 1 4.0E-03
CUI: C1867864
Disease: Poor fine motor coordination
Poor fine motor coordination 		0 3 0 0 1 4.0E-03
CUI: C3714745
Disease: Malabsorption
Malabsorption 		0 3 0 0 1 4.0E-03
CUI: C3806402
Disease: EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION 		0 23 0 0 1 3.7E-03
CUI: C4025792
Disease: EEG with irregular generalized spike and wave complexes
EEG with irregular generalized spike and wave complexes 		0 1 0 0 1 4.1E-03
CUI: C4317045
Disease: Gluten intolerance
Gluten intolerance 		0 1 0 0 1 4.1E-03
CUI: C4693362
Disease: EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2
EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2 		0 6 0 0 1 4.0E-03
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		9 0 1 6.0E-03 0 0
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		1 0 1 6.3E-03 0 0
CUI: C0002886
Disease: Anemia, Macrocytic
Anemia, Macrocytic 		1 1 1 6.3E-03 1 4.1E-03
CUI: C0003079
Disease: Anisocoria
Anisocoria 		4 0 1 6.1E-03 0 0
CUI: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis 		3 0 1 6.2E-03 0 0
CUI: C0003537
Disease: Aphasia
Aphasia 		2 2 1 6.2E-03 1 4.0E-03
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation 		3 0 1 6.2E-03 0 0
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		5 0 1 6.1E-03 0 0
CUI: C0004158
Disease: Athetosis
Athetosis 		2 0 1 6.2E-03 0 0
CUI: C0004779
Disease: Basal Cell Nevus Syndrome
Basal Cell Nevus Syndrome 		3 117 1 6.2E-03 1 2.8E-03
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		5 0 1 6.1E-03 0 0
CUI: C0005741
Disease: Blepharitis
Blepharitis 		3 0 1 6.2E-03 0 0
CUI: C0006009
Disease: Borderline intellectual disability
Borderline intellectual disability 		3 3 1 6.2E-03 1 4.0E-03