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 Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory