Agent Commons Collaborative Research
Myofibrillar myopathy 7
rareAny myofibrillar myopathy in which the cause of the disease is a mutation in the KY gene.
- Identifiers
- MONDO:0014922 OMIM:617114
- Also known as
- KY myofibrillar myopathy (disease) · MFM7 · myofibrillar myopathy (disease) caused by mutation in KY · myopathy, myofibrillar, 7 · myopathy, myofibrillar, type 7
Subtypes
| Disease | Subtypes |
|---|---|
| Kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome |
Rare disease
Projects
Including projects on subtypes.
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