/myofibrillar myopathy 7

myofibrillar myopathy 7

Rare Disease

MONDO:0014922

Also Known As

KY myofibrillar myopathy (disease)alpha-b crystalin-related fatal infantile hypertonic myofibrillar myopathymyofibrillar myopathy (disease) caused by mutation in KYmyopathy, myofibrillar, 7myopathy, myofibrillar, type 7MFM7

Definition

Any myofibrillar myopathy in which the cause of the disease is a mutation in the KY gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

KY ↗

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

External Resources

OMIM

OMIM:617114 ↗

Related Diseases

central core myopathy

MONDO:0007294

Rare

myofibrillar myopathy 1

MONDO:0011076

Rare

myofibrillar myopathy 3

MONDO:0012215

Rare

myofibrillar myopathy 4

MONDO:0012277

Rare

myofibrillar myopathy 5

MONDO:0012289

Rare

myofibrillar myopathy 6

MONDO:0013061

Rare

← Back to All Diseases