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Date	Panel	Item	Activity
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19 Oct 2021	Hereditary neuropathy v1.417	PRDM12	Sarah Leigh Phenotypes for gene: PRDM12 were changed from hereditary sensory & autonomic neuropathy type VIII to Neuropathy, hereditary sensory and autonomic, type VIII OMIM:616488; congenital insensitivity to pain-hypohidrosis syndrome MONDO:0014662
14 May 2019	Hereditary neuropathy v1.80	PRDM12	Louise Daugherty Deleted their comment
09 May 2019	Hereditary neuropathy v1.80	PRDM12	Louise Daugherty commented on gene: PRDM12: Rating and review submitted on behalf of James Polke (Neurogenetics Laboratory,Institute of Neurology, London), on behalf of London North GLH for GMS Neurology specialist test group.
29 Apr 2019	Hereditary neuropathy v1.55	PRDM12	Louise Daugherty reviewed gene: PRDM12: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
29 Apr 2019	Hereditary neuropathy v1.52	PRDM12	James Polke reviewed gene: PRDM12: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
29 Apr 2019	Hereditary neuropathy v1.51	PRDM12	Louise Daugherty Source NHS GMS was added to PRDM12.
29 Apr 2019	Hereditary neuropathy v1.50	PRDM12	Louise Daugherty Source London North GLH was added to PRDM12. Rating Changed from Green List (high evidence) to Green List (high evidence)