Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0033300
Disease: Progeria
Progeria
1.000 GeneticVariation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0033300
Disease: Progeria
Progeria
1.000 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
1.000 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
0.920 GeneticVariation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
0.920 Biomarker CTD_human

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
0.920 CausalMutation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
0.920 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Charcot-Marie-Tooth disease, Type 2B1
0.900 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Charcot-Marie-Tooth disease, Type 2B1
0.900 Biomarker CTD_human

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
0.800 GermlineCausalMutation ORPHANET

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
0.800 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis
0.800 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis
0.800 CausalMutation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Familial Partial Lipodystrophy, Type 2
0.800 GeneticVariation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Familial Partial Lipodystrophy, Type 2
0.800 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome
0.710 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome
0.710 Biomarker CTD_human

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome
0.710 CausalMutation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Lethal tight skin contracture syndrome (disorder)
0.700 Biomarker CTD_human

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Lethal tight skin contracture syndrome (disorder)
0.700 CausalMutation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Lethal tight skin contracture syndrome (disorder)
0.700 Biomarker GENOMICS_ENGLAND

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss
0.700 Biomarker MGD

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss
0.700 CausalMutation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss
0.700 GeneticVariation CLINVAR

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
0.700 Biomarker HPO