Disease

hereditary sensory neuropathy type 1D

Definition
A hereditary sensory and autonomic neuropathy type 1 characterized dult onset of a distal axonal sensory neuropathy affecting all modalities, often associated with distal ulceration and amputation as well as hyporeflexia, although some patients may show features suggesting upper neuron involvement that has_material_basis_in heterozygous mutation in the ATL1 gene on chromosome 14q.
Synonyms
  • HSN1D
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

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Associated Models