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autosomal recessive limb-girdle muscular dystrophy type 2J

MeSH: C563854ORPHA: 140922

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous mutation in the titin gene (TTN)

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C563854

Orphanet Code

ORPHA:140922
autosomal recessive limb-girdle muscular dystrophy type 2J
MeSHC563854
OrphanetORPHA:140922
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
autosomal recessive limb-girdle muscular dystrophy type 2J | OrphanDrug