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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: Apr 21, 2024
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Records 1 - 21 (of 21 Records)
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Anemia[original query]>>Evidence Synthesis [Product Type]
Epidemiology of Glucose-6-Phosphate Dehydrogenase Deficiency in Arab Countries: Insights from a Systematic Review.
Abdulaziz S Alangari et al. J Clin Med 2023 12(20)
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Predicting perinatal mortality based on maternal health status and health insurance service using homogeneous ensemble machine learning methods.
Bogale Dawit S et al. BMC medical informatics and decision making 2022 22(1) 341
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Manifestations of HbSE sickle cell disease: a systematic review.
Khamees Ibrahim et al. Journal of translational medicine 2021 19(1) 262
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Pediatric Neurodevelopmental Delays in Children 0 to 5 Years of Age With Sickle Cell Disease: A Systematic Literature Review.
Knight La'Kita M J et al. Journal of pediatric hematology/oncology 2021 Feb
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CLINGEN Actionability Report for Familial Adenomatous Polyposis - APC
ClinGen Actionability Working Group
CLINGEN Actionability Report for Hereditary Hemorrhagic Telangiectasia - ENG, ACVRL1, SMAD4, GDF2
ClinGen Actionability Working Group
CLINGEN Actionability Report for Peutz-Jeghers Syndrome - STK11
ClinGen Actionability Working Group
CLINGEN Actionability Report for Acrodermatitis enteropathica, zinc-deficiency type-SLC39A4
ClinGen Actionability Working Group
CLINGEN Actionability Report for WAS-related disorders-WAS
ClinGen Actionability Working Group
CLINGEN Actionability Report for Wilms tumor-WT1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Juvenile polyposis syndrome - SMAD4, BMPR1A
ClinGen Actionability Working Group
CLINGEN Actionability Report for Aceruloplasminemia-CP
ClinGen Actionability Working Group
CLINGEN Actionability Report for Wilson Disease - ATP7B
ClinGen Actionability Working Group
CLINGEN Actionability Report for Paragangliomas 1, 2, 3, 4, 5; Pheochromocytoma- MAX, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127
ClinGen Actionability Working Group
CLINGEN Actionability Report for Hereditary Diffuse Gastric Cancer - CDH1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Gaucher Disease - GBA
ClinGen Actionability Working Group
A Cost-Effectiveness Analysis of a Pilot Neonatal Screening Program for Sickle Cell Anemia in the Republic of Angola.
McGann Patrick T et al. The Journal of pediatrics 2015 Dec 167(6) 1314-9
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Prevalence, genetic variants and clinical implications of G-6-PD deficiency in Burkina Faso: a systematic review.
Ouattara Abdoul Karim et al. BMC medical genetics 2017 18(1) 139
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Hydroxyurea for hemoglobin E/β-thalassemia: a systematic review and meta-analysis.
Algiraigri Ali H et al. International journal of hematology 2017 Aug
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A systematic review of the literature for severity predictors in children with sickle cell anemia.
Meier Emily Riehm et al. Blood cells, molecules & diseases 2017 Feb
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Clinical utility gene card for: Diamond-Blackfan anemia--update 2013.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 21, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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