Diseases

Laminopathies

Congenital neuromuscular and muscular dystrophy diseases associated with mutations in the LAMIN TYPE A (Lamin A/C or LMNA gene). It includes CARDIOMYOPATHY, DILATED, 1A; CHARCOT-MARIE-TOOTH DISEASE, type 2B1; EMERY-DREIFUSS MUSCULAR DYSTROPHY, types 2 and 3; HUTCHINSON-GILFORD PROGERIA SYNDROME; LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; Malouf syndrome; Mandibuloacral dysplasia; LMNA-related muscular dystrophy; Restrictive dermopathy, lethal; Heart-hand syndrome, Slovenian type.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

Congenital neuromuscular and muscular dystrophy diseases associated with mutations in the LAMIN TYPE A (Lamin A/C or LMNA gene). It includes CARDIOMYOPATHY, DILATED, 1A; CHARCOT-MARIE-TOOTH DISEASE, type 2B1; EMERY-DREIFUSS MUSCULAR DYSTROPHY, types 2 and 3; HUTCHINSON-GILFORD PROGERIA SYNDROME; LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; Malouf syndrome; Mandibuloacral dysplasia; LMNA-related muscular dystrophy; Restrictive dermopathy, lethal; Heart-hand syndrome, Slovenian type.

MeSH Record

Classification

Broader headings

Narrower headings

Related Concepts

Knowledge Graph

Loading graph…

Drag nodes to rearrange; hover to trace links; click a node to open its page.

MeSH Record

Synonyms

9 entry terms
  • LMNA-Associated Diseases
  • LMNA-Linked Diseases
  • Disease, LMNA-Associated
  • Disease, LMNA-Linked
  • LMNA Associated Diseases
  • LMNA Linked Diseases
  • LMNA-Associated Disease
  • LMNA-Linked Disease
  • Laminopathy

MeSH Record

Aspects Covered

34 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

History Note

2021

MeSH Record

Previous Indexing

  • Cardiomyopathies (2002-2020)
  • Lamin Type A/genetics (2002-2020)
  • Neuromuscular Diseases (2002-2020)

MeSH Hierarchy

Tree Number

  1. C16w.320w.488w

AMA Style

References

  1. National Library of Medicine. Laminopathies. Medical Subject Headings (MeSH). 2026. Unique ID D000083083. http://id.nlm.nih.gov/mesh/2026/D000083083
  2. Laminopathies. In: Wikipedia. https://en.wikipedia.org/wiki/Laminopathy
  3. Laminopathies. In: Wikidata. https://www.wikidata.org/wiki/Q3216770