/congenital myopathy 7A, myosin storage, autosomal dominant

congenital myopathy 7A, myosin storage, autosomal dominant

Rare Disease

MONDO:0008409

Also Known As

MSMAMYH7-related late-onset SPMDMYH7-related late-onset scapuloperoneal muscular dystrophyMYH7-related late-onset scapuloperoneal syndromeMYH7-related scapuloperoneal myopathySPMDSPMMautosomal dominant myosin storage myopathymyopathy with lysis of type 1 myofibrilsmyopathy, hyaline body, autosomal dominantmyopathy, myosin storage, autosomal dominantscapuloperoneal muscular dystrophyscapuloperoneal myopathy, MYH7-relatedscapuloperoneal syndrome, myopathic type

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

MYH7 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

Related Diseases

polymicrogyria

MONDO:0000087

Rare

congenital myasthenic syndrome with tubular aggregates

MONDO:0000182

Rare

prenatal-onset spinal muscular atrophy with congenital bone fractures

MONDO:0000209

Rare

anencephaly

MONDO:0000819

cerebral cavernous malformation

MONDO:0000820

meningocele

MONDO:0001147

← Back to All Diseases

congenital myopathy 7A, myosin storage, autosomal dominant

Also Known As

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases