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DO Term : hereditary sensory and autonomic neuropathy type 8 [DOID:0070153] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary sensory neuropathy characterized by congenital insensitivity to pain and decreased sweating and tear production that has_material_basis_in homozygous mutation in the PRDM12 gene on chromosome 9q34.
  • synonyms:
  • 616488,
  • ORDO:478664,
  • hereditary sensory and autonomic neuropathy type VIII,
  • HSAN8,
  • OMIM:616488
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