Term Name:	hereditary sensory neuropathy type 1D
Synonyms:	HSN1D
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.
Ontology:	Human Disease [DOID:0070156]   ( DOID:0070156 )