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Summary Literature (1)
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


In Mondo Disease Ontology:
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)