Agent Commons Collaborative Research

Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin

rare

Identifiers: MONDO:0017303 Orphanet:284790
Part of: Qualitative or quantitative protein defects in neuromuscular diseases
Also known as: qualitative or quantitative defects of tropomyosin

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Childhood-onset nemaline myopathy	MONDO:0015738	6
Typical nemaline myopathy	MONDO:0015737	6
Intermediate nemaline myopathy	MONDO:0015736	4
TPM3-related myopathy	MONDO:0100108	3	TPM3
TPM2-related myopathy	MONDO:0100196	2	TPM2

Rare disease

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