DOID:0070153 - hereditary sensory and autonomic neuropathy type 8
Disease Ontology Definition:A hereditary sensory neuropathy characterized by congenital insensitivity to pain and decreased sweating and tear production that has_material_basis_in homozygous mutation in the PRDM12 gene on chromosome 9q34.
Synonyms: HSAN8, hereditary sensory and autonomic neuropathy type VIII
|MONDO:0014662 - congenital insensitivity to pain-hypohidrosis syndrome|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : prdm12
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hereditary sensory neuropathy (is_a)