About   Help   FAQ
Disease Ontology Browser
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory