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: C0033300
Disease: Progeria
Progeria 		1 20 1 1.00 2 9.1E-02
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 1.00 0 0
CUI: C0264906
Disease: Second degree atrioventricular block
Second degree atrioventricular block 		1 0 1 1.00 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		1 0 1 1.00 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		1 3 1 1.00 2 0.40
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 25 1 1.00 2 7.4E-02
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		1 8 1 1.00 2 0.20
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 4 1 1.00 2 0.33
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		1 17 1 1.00 2 0.11
CUI: C1834653
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder) 		1 4 1 1.00 1 0.14
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 3 1 1.00 2 0.40
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 1.00 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 13 1 1.00 2 0.13
CUI: C4016241
Disease: HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL 		1 0 1 1.00 0 0
CUI: C4229131
Disease: Distal acroosteolysis
Distal acroosteolysis 		1 0 1 1.00 0 0
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy 		2 0 1 0.50 0 0
CUI: C0406585
Disease: Lethal tight skin contracture syndrome (disorder)
Lethal tight skin contracture syndrome (disorder) 		2 10 1 0.50 2 0.17
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature 		2 0 1 0.50 0 0
CUI: C0162298
Disease: Joint stiffness
Joint stiffness 		3 0 1 0.33 0 0
CUI: C1843392
Disease: Death in childhood
Death in childhood 		3 0 1 0.33 0 0
CUI: C1854154
Disease: Charcot-Marie-Tooth disease, Type 2B1
Charcot-Marie-Tooth disease, Type 2B1 		3 6 1 0.33 2 0.25
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		3 0 1 0.33 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		4 0 1 0.25 0 0
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		4 26 1 0.25 2 7.1E-02
CUI: C2063326
Disease: Right ventricular cardiomyopathy
Right ventricular cardiomyopathy 		4 0 1 0.25 0 0