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GTR Home > Conditions/Phenotypes > Autosomal dominant slowed nerve conduction velocity

Autosomal dominant slowed nerve conduction velocity

Summary

A hereditary demyelinating motor and sensory neuropathy with characteristics of slowed nerve conduction velocities in the absence of clinically apparent neurological deficits, gait abnormalities or muscular atrophy, associated with a germline mutation in the ARGHEF10 gene. [from SNOMEDCT_US]

Available tests

10 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: GEF10, SNCV, ARHGEF10
    Summary: Rho guanine nucleotide exchange factor 10

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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