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: C0037188
Disease: Sinoatrial Block
Sinoatrial Block
1 0 1 1.00 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome
1 4 1 1.00 2 0.40
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome
1 0 1 1.00 0 0
Charcot-Marie-Tooth disease, Type 2B1
1 6 1 1.00 2 0.29
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3
1 4 1 1.00 2 0.40
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
1 19 1 1.00 2 1.0E-01
CUI: C4275075
Disease: Atypical Werner syndrome
Atypical Werner syndrome
1 0 1 1.00 0 0
LMNA-related cardiocutaneous progeria syndrome
1 0 1 1.00 0 0
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block
2 0 1 0.50 0 0
Lethal tight skin contracture syndrome (disorder)
2 10 1 0.50 2 0.18
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis
2 8 1 0.50 2 0.22
HIV-Associated Lipodystrophy Syndrome
2 0 1 0.50 0 0
CUI: C0036420
Disease: Localized scleroderma
Localized scleroderma
3 0 1 0.33 0 0
CUI: C0263409
Disease: Linear Scleroderma
Linear Scleroderma
3 0 1 0.33 0 0
CUI: C1527383
Disease: Morphea
Morphea
3 0 1 0.33 0 0
CUI: C0004331
Disease: Auriculo-Ventricular Dissociation
Auriculo-Ventricular Dissociation
4 0 1 0.25 0 0
CUI: C0011644
Disease: Scleroderma
Scleroderma
4 0 1 0.25 0 0
CUI: C0016508
Disease: Congenital Foot Deformity
Congenital Foot Deformity
4 0 1 0.25 0 0
CUI: C0018794
Disease: Heart Block
Heart Block
4 0 1 0.25 0 0
CUI: C0033300
Disease: Progeria
Progeria
5 27 1 0.20 2 7.1E-02
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
5 71 1 0.20 2 2.8E-02
Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
5 0 1 0.20 0 0
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
5 0 1 0.20 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss
6 0 1 0.17 0 0
X-Linked Emery-Dreifuss Muscular Dystrophy
7 0 1 0.14 0 0