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Summary Literature (1)
MIM:616488 - NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8


Xenbase Genes: prdm12

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014662 - congenital insensitivity to pain-hypohidrosis syndrome

Disease Ontology (DO):
DOID:0070153 - hereditary sensory and autonomic neuropathy type 8