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hereditary sensory and autonomic neuropathy type 6 (DOID:0070151)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type VI; HSAN6
Alt IDs: ICD10CM:G60.8, OMIM:614653, 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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MGI 6.13
The Jackson Laboratory