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neuronopathy, distal hereditary motor, type 2A | RareConnect | RareConnect.io

/distal hereditary motor neuropathy type 2

/neuronopathy, distal hereditary motor, type 2A

neuronopathy, distal hereditary motor, type 2A

Rare Disease

MONDO:0008025

Also Known As

HSPB8 neuronopathy, distal hereditary motorneuronopathy, distal hereditary motor caused by mutation in HSPB8Charcot-Marie-Tooth disease, spinal, 2AHMN 2AHMN2Aneuronopathy, distal hereditary motor, type IIAneuropathy, distal hereditary motor, type 2Aspinal muscular atrophy, distal, adult, autosomal dominant, 2A

Definition

Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB8 gene.

Patient-Friendly Information

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:158590 ↗

GARD

Related Diseases

neuronopathy, distal hereditary motor, type 2B

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neuronopathy, distal hereditary motor, type 2C

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neuronopathy, distal hereditary motor, type 2D

MONDO:0014259

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