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: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2 		1 0 1 2.2E-02 0 0
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology 		1 0 1 2.2E-02 0 0
CUI: C4021803
Disease: Abnormal eyelid morphology
Abnormal eyelid morphology 		3 0 2 4.3E-02 0 0
CUI: C4531288
Disease: Abnormal morphology of left ventricular trabeculae
Abnormal morphology of left ventricular trabeculae 		1 0 1 2.2E-02 0 0
CUI: C4022648
Disease: Abnormal muscle fiber dystrophin expression
Abnormal muscle fiber dystrophin expression 		1 0 1 2.2E-02 0 0
CUI: C4021264
Disease: Abnormal ventricular septum morphology
Abnormal ventricular septum morphology 		1 0 1 2.2E-02 0 0
CUI: C4023612
Disease: Abnormality of cellular immune system
Abnormality of cellular immune system 		4 0 1 2.1E-02 0 0
CUI: C4023166
Disease: Abnormality of T cell physiology
Abnormality of T cell physiology 		4 0 1 2.1E-02 0 0
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature 		2 0 1 2.2E-02 0 0
CUI: C0241657
Disease: Abnormality of the vasculature
Abnormality of the vasculature 		2 2 1 2.2E-02 1 5.8E-03
CUI: C4703449
Disease: Aborted sudden cardiac death
Aborted sudden cardiac death 		1 0 1 2.2E-02 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		11 0 2 3.7E-02 0 0
CUI: C4317146
Disease: Acid reflux
Acid reflux 		50 0 1 1.1E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		9 14 1 1.9E-02 3 1.6E-02
CUI: C0702166
Disease: Acne
Acne 		3 0 2 4.3E-02 0 0
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		1 0 1 2.2E-02 0 0
CUI: C1837317
Disease: Alpha-B Crystallinopathy
Alpha-B Crystallinopathy 		1 0 1 2.2E-02 0 0
CUI: C3151471
Disease: AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED
AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED 		1 1 1 2.2E-02 1 5.8E-03
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED 		1 43 1 2.2E-02 3 1.4E-02
CUI: C3151470
Disease: AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED 		1 0 1 2.2E-02 0 0
CUI: C0002871
Disease: Anemia
Anemia 		11 14 1 1.8E-02 1 5.4E-03
CUI: C0152415
Disease: Ankyloglossia
Ankyloglossia 		2 0 1 2.2E-02 0 0
CUI: C0750929
Disease: Arnold-Chiari Malformation, Type I
Arnold-Chiari Malformation, Type I 		1 0 1 2.2E-02 0 0
CUI: C0349788
Disease: Arrhythmogenic Right Ventricular Dysplasia
Arrhythmogenic Right Ventricular Dysplasia 		11 108 7 0.14 6 2.2E-02
CUI: C1857777
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 		2 27 2 4.4E-02 1 5.1E-03