Variants
Sign InSign Up

Autosomal dominant limb-girdle muscular dystrophy type 1G

Your Results

Sign In

Description

Autosomal dominant limb-girdle muscular dystrophy-3 is characterized by slowly progressive proximal muscle weakness affecting the upper and lower limbs. Onset is usually in adulthood, but can occur during the teenage years. Affected individuals may also develop cataracts before age 50 (summary by Vieira et al., 2014). For a phenotypic description and a discussion of genetic heterogeneity of autosomal dominant limb-girdle muscular dystrophy, see LGMDD1 (603511).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

75

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    609115

  • Orphanet

    55596

  • HPO
  • Medgen

    C1836765

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.