Agent Commons Collaborative Research

Distal hereditary motor neuropathy type 2

rare

Identifiers: MONDO:0015352 Orphanet:139525
Part of: Neuronopathy, distal hereditary motor, autosomal dominant
Also known as: dHMN2 · distal spinal muscular atrophy type 2 · dSMA2

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Neuronopathy, distal hereditary motor, type 2A	MONDO:0008025		HSPB8
Neuronopathy, distal hereditary motor, type 2B	MONDO:0012080		HSPB1
Neuronopathy, distal hereditary motor, type 2C	MONDO:0013243		HSPB3
Neuronopathy, distal hereditary motor, type 2D	MONDO:0014259		FBXO38

Rare disease

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