hereditary sensory neuropathy type 1D (DOID:0070156)
Alliance: disease page
Synonyms: HSN1D
Alt IDs: OMIM:613708
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.