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MIM:616488 - NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8
Xenbase Genes: prdm12
Human Disease Resource: MIM
MONDO:0014662 - congenital insensitivity to pain-hypohidrosis syndrome |
DOID:0070153 - hereditary sensory and autonomic neuropathy type 8 |