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: C0007279
Disease: Carotid Body Paraganglioma
Carotid Body Paraganglioma 		1 0 1 2.2E-02 0 0
CUI: C0007286
Disease: Carpal Tunnel Syndrome
Carpal Tunnel Syndrome 		1 3 1 2.2E-02 2 1.2E-02
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		1 151 1 2.2E-02 1 3.1E-03
CUI: C0018794
Disease: Heart Block
Heart Block 		1 0 1 2.2E-02 0 0
CUI: C0033300
Disease: Progeria
Progeria 		1 0 1 2.2E-02 0 0
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 2.2E-02 0 0
CUI: C0086769
Disease: Panic Attacks
Panic Attacks 		1 1 1 2.2E-02 1 5.8E-03
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy 		1 0 1 2.2E-02 0 0
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		1 0 1 2.2E-02 0 0
CUI: C0239574
Disease: Low grade fever
Low grade fever 		1 0 1 2.2E-02 0 0
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart 		1 0 1 2.2E-02 0 0
CUI: C0264906
Disease: Second degree atrioventricular block
Second degree atrioventricular block 		1 0 1 2.2E-02 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		1 0 1 2.2E-02 0 0
CUI: C0344975
Disease: Pulmonary Atresia with Intact Ventricular Septum
Pulmonary Atresia with Intact Ventricular Septum 		1 0 1 2.2E-02 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		1 0 1 2.2E-02 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		1 0 1 2.2E-02 0 0
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 0 1 2.2E-02 0 0
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		1 0 1 2.2E-02 0 0
CUI: C0520806
Disease: Unexplained sudden death
Unexplained sudden death 		1 0 1 2.2E-02 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2 		1 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: C0795905
Disease: Cantu syndrome
Cantu syndrome 		1 0 1 2.2E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 2.2E-02 0 0
CUI: C0878677
Disease: Glycogen Storage Disease Type IIb
Glycogen Storage Disease Type IIb 		1 37 1 2.2E-02 1 4.8E-03
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		1 28 1 2.2E-02 1 5.0E-03