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: 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: C0007642
Disease: Cellulitis
Cellulitis 		1 1 1 6.3E-03 1 4.1E-03
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities 		1 0 1 6.3E-03 0 0
CUI: C0008373
Disease: Cholesteatoma
Cholesteatoma 		1 1 1 6.3E-03 1 4.1E-03
CUI: C0009681
Disease: Anomalous pulmonary artery
Anomalous pulmonary artery 		1 0 1 6.3E-03 0 0
CUI: C0010043
Disease: Corneal Ulcer
Corneal Ulcer 		1 0 1 6.3E-03 0 0
CUI: C0010051
Disease: Coronary Aneurysm
Coronary Aneurysm 		1 0 1 6.3E-03 0 0
CUI: C0010520
Disease: Cyanosis
Cyanosis 		1 1 1 6.3E-03 1 4.1E-03
CUI: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis 		1 1 1 6.3E-03 1 4.1E-03
CUI: C0015930
Disease: Fetal Distress
Fetal Distress 		1 1 1 6.3E-03 1 4.1E-03
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		1 0 1 6.3E-03 0 0
CUI: C0020500
Disease: Hyperoxaluria
Hyperoxaluria 		1 1 1 6.3E-03 1 4.1E-03