OrphanDrug
OrphanDrug
Pharma Knowledge Base

congenital muscular dystrophy due to integrin alpha-7 deficiency

MeSH: C567709ORPHA: 34520

Contents

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

Overview

congenital muscular dystrophy characterized by autosomal recessive inheritance that has material basis in compound heterozygous mutation in the ITGA7 gene on chromosome 12q13

Available Treatments (0)

No treatments linked yet

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

Classification & Codes

MeSH Code

C567709

Orphanet Code

ORPHA:34520
congenital muscular dystrophy due to integrin alpha-7 deficiency
MeSHC567709
OrphanetORPHA:34520
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO