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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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Public Health Genomics Branch
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CDC/NIH Web Information Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: Sep 16, 2024
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Records 1-30 (of 56 Records)
CDC/NIH Web Information
The Use of Cell-free DNA in Clinical Practice: Work in Progress
M Clyne et al, CDC Blog Post, December 14, 2022
5 Things You Should Know About Epilepsy
CDC, November 2022
Sudden Unexpected Death in Epilepsy (SUDEP)
CDC, 2019
Epilepsy in Children
CDC, August 2019
Epilepsy and Seizures in Older Adults
Epilepsy: Improving Quality of Life
Loving Someone With Epilepsy
E Sharmin, Public Health Matters Blog, Nov 1, 2017
5 Things You Should Know About Epilepsy
Study finds genetic basis for drug response in childhood absence epilepsy
NIH Press Release, April 11, 2017
Spotlight on Seizures
Epilepsy: Frequently Asked Questions
Epilepsy and Seizures in Older Adults
Seizure First Aid
Epilepsia
November is National Epilepsy Awareness Month
Seizures in Children and Adolescents Aged 617 Years United States, 20102014
W Cui et al, MMWR, November 6, 2015
Epilepsy often comes with other health issues
Epilepsy: Frequently asked questions
Epilepsy
CDC Information: Managing Epilepsy
Pachygyria-intellectual disability-epilepsy syndrome
From NCATS Genetic and Rare Diseases Information Center
Alopecia epilepsy oligophrenia syndrome of Moynahan
From NCATS Genetic and Rare Diseases Information Center
Alopecia, epilepsy, pyorrhea, mental subnormality
From NCATS Genetic and Rare Diseases Information Center
Benign familial infantile epilepsy
From NCATS Genetic and Rare Diseases Information Center
Benign familial neonatal epilepsy
From NCATS Genetic and Rare Diseases Information Center
Epilepsy juvenile absence
From NCATS Genetic and Rare Diseases Information Center
Epilepsy mental deterioration Finnish type
From NCATS Genetic and Rare Diseases Information Center
Epilepsy occipital calcifications
From NCATS Genetic and Rare Diseases Information Center
Epilepsy progressive myoclonic type 3
From NCATS Genetic and Rare Diseases Information Center
Epilepsy telangiectasia
From NCATS Genetic and Rare Diseases Information Center
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Page last reviewed:
Feb 1, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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