autosomal recessive limb-girdle muscular dystrophy type 2M

MeSH: C566912ORPHA: 206554

Contents

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

Overview

autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31

Available Treatments (0)

No treatments linked yet

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

Classification & Codes

MeSH Code

C566912

Orphanet Code

ORPHA:206554

autosomal recessive limb-girdle muscular dystrophy type 2M

MeSH	`C566912`
Orphanet	`ORPHA:206554`
Treatments	0 drug(s)
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO