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 1F ID (Ontology) DOID:0070154 (Human Disease)
Definition A hereditary sensory and autonomic neuropathy type 1 characterized by distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13.
Also Known As "hereditary sensory neuropathy type IF" ; "HSN1F"
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 Genes
 hereditary sensory neuropathy type 1F       1
 for disease ribbon | hereditary sensory neuropathy type 1F       1
 model of | hereditary sensory neuropathy type 1F       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 1F  1 rec.
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Is a autosomal dominant disease
hereditary sensory and autonomic neuropathy type 1
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Synonyms
  • "hereditary sensory neuropathy type IF" EXACT
    "HSN1F" EXACT OMO:0003012
Secondary IDs
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MIM:615632