About   Help   FAQ
Disease Ontology Browser
hereditary sensory and autonomic neuropathy type 6 (DOID:0070151)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type VI; HSAN6
Alt IDs: OMIM:614653, ICD10CM:G60.8, ORDO:314381
Definition: A hereditary sensory neuropathy characterized by neonatal hypotonia, respiratory and feeding difficulties, impaired psychomotor development, and autonomic abnormalities that has_material_basis_in homozygous mutation in the DST gene on chromosome 6p12.

Disease References using Mouse Models (1)

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
01/24/2023
MGI 6.22
The Jackson Laboratory