has material basis in germline mutation in disease shares features of LMNA X-linked Emery-Dreifuss muscular dystrophy muscular dystrophy, limb-girdle, autosomal dominant autosomal dominant Emery-Dreifuss muscular dystrophy Emery-Dreifuss muscular dystrophy 2, autosomal dominant https://rarediseases.info.nih.gov/diseases/10230/limb-girdle-muscular-dystrophy-type-1b proximal muscular dystrophy type 1B NCIT:C126745 EDMD2 muscular dystrophy, limb-girdle type 1B DOID:0110301 benign scapuloperoneal muscular dystrophy with cardiomyopathy EMD2 GARD:0010230 autosomal dominant limb-girdle muscular dystrophy caused by mutation in LMNA SCTID:718178006 LMNA autosomal dominant limb-girdle muscular dystrophy DOID:0070247 Orphanet:264 MEDGEN:98048 UMLS:C0410190 Hauptmann-Thannhauser muscular dystrophy muscular dystrophy, limb-girdle, type 1B Emery-Dreifuss muscular dystrophy 2, autosomal dominant ICD9:425.4 MONDO:0021569 LGMD1B limb-girdle muscular dystrophy type 1B OMIM:181350 OMIM:159001 limb-girdle muscular dystrophy due to lamin A/C deficiency MESH:C535898 Emery-Dreifuss muscular dystrophy inherited in an autosomal dominant pattern and caused by mutations in the LMNA gene. SCTID:240072005 muscular dystrophy, proximal, type 1B