Summary Literature (0)

DOID:0070151 - hereditary sensory and autonomic neuropathy type 6

Disease Ontology 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.

Synonyms: HSAN6, hereditary sensory and autonomic neuropathy type VI,

Echinobase Genes :


OMIM:

MIM:614653 - neuropathy, hereditary sensory and autonomic, type vi; hsan6

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee