FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary sensory neuropathy type 1D ID (Ontology) DOID:0070156 (Human Disease)
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.
Also Known As "HSN1D"
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 Genes
 hereditary sensory neuropathy type 1D       1
 for disease ribbon | hereditary sensory neuropathy type 1D       1
 model of | hereditary sensory neuropathy type 1D       1
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hereditary sensory neuropathy
 |__hereditary sensory and autonomic neuropathy type 1__
autosomal genetic disease                               |
 |__autosomal dominant disease__________________________|
                                                        hereditary sensory neuropathy type 1D  1 rec.
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Is a autosomal dominant disease
hereditary sensory and autonomic neuropathy type 1
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Synonyms
  • "HSN1D" EXACT OMO:0003012
Secondary IDs
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MIM:613708