KY-related neuromyopathy

rare

Any neuromyopathy in which the cause of the disease is mutation in the KY gene.

Subtypes

Disease	ID	Subtypes
Myofibrillar myopathy 7	MONDO:0014922	1
Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome	MONDO:0044648

Rare disease

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