FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term hereditary sensory and autonomic neuropathy type 1 ID (Ontology) DOID:0070162 (Human Disease)
Definition A hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance.
Also Known As "hereditary sensory and autonomic neuropathy type I" ; "HSAN1"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       9
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 hereditary sensory and autonomic neuropathy type 1       9      2
 model of | hereditary sensory and autonomic neuropathy type 1       9       --
Spanning Tree (Parents/Children)
Only view relationship: 
  neuropathy
   |__hereditary sensory neuropathy
       |__hereditary sensory and autonomic neuropathy type 1  14 rec.
           |__hereditary sensory and autonomic neuropathy type 1A 5 rec.
           |__hereditary sensory and autonomic neuropathy type 1C 2 rec.
           |__hereditary sensory neuropathy type 1D 1 rec.
           |__hereditary sensory neuropathy type 1F 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a hereditary sensory neuropathy
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "hereditary sensory and autonomic neuropathy type I" EXACT
    "HSAN1" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
GARD:6635
MESH:D009477
NCI:C170433
ORDO:36386
SNOMEDCT_US_2023_03_01:52647008
UMLS_CUI:C0020071