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hereditary sensory and autonomic neuropathy type 8 (DOID:0070153)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type VIII; HSAN8
Alt IDs: OMIM:616488, ORDO:478664
Definition: 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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/17/2023
MGI 6.22
The Jackson Laboratory