Autosomal dominant titinopathy

rare

Autosomal dominant form of TTN-related myopathy.

Subtypes

Disease	ID	Subtypes
TTN-related myopathy, dominant-negative TTNsv	MONDO:1060225
Dilated cardiomyopathy 1G	MONDO:0011400
Hypertrophic cardiomyopathy 9	MONDO:0013412
Myopathy, myofibrillar, 9, with early respiratory failure	MONDO:0011362
Tibial muscular dystrophy	MONDO:0010870

Rare disease

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