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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)
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last database update
02/18/2020
MGI 6.14
The Jackson Laboratory