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Genes and Genomic Entities
CCNF
CCNF
cyclin F
OMIM: 600227
,
Gene2Phenotype
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CCNF
in
Adult onset neurodegenerative disorder
Version 4.47
Latest signed off version:
v4.34
(31 Jul 2023)
review
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
Yorkshire and North East GLH
Expert Review Green
NHS GMS
London North GLH
Phenotypes
Frontotemporal dementia and/or amyotrophic lateral sclerosis 5, OMIM:619141