FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary sensory and autonomic neuropathy type 7 ID (Ontology) DOID:0070149 (Human Disease)
Definition A hereditary sensory neuropathy characterized by insensitivity to pain, mild muscle weakness, delayed motor development, hyperhidrosis and gastrointestinal dysfunction that has_material_basis_in heterozygous mutation in the SCN11A gene on chromosome 3p22.
Also Known As "hereditary sensory and autonomic neuropathy type VII" ; "HSAN7"
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 Genes
 hereditary sensory and autonomic neuropathy type 7       2
 for disease ribbon | hereditary sensory and autonomic neuropathy type 7       2
 model of | hereditary sensory and autonomic neuropathy type 7       2
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autosomal genetic disease
 |__autosomal dominant disease_____
neuropathy                         |
 |__hereditary sensory neuropathy__|
                                   hereditary sensory and autonomic neuropathy type 7  2 rec.
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Is a hereditary sensory neuropathy
autosomal dominant disease
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Synonyms
  • "hereditary sensory and autonomic neuropathy type VII" EXACT
    "HSAN7" EXACT OMO:0003012
Secondary IDs
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GARD:12723
ICD10CM:G60.8
MIM:615548
ORDO:391397