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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,
Xenbase Genes : dst
MONDO:0013839 - hereditary sensory and autonomic neuropathy type 6 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hereditary sensory neuropathy (is_a)