Typhus
What's New
Last Posted: Nov 16, 2023
- Identification of novel variants for complicating cardiac disease in the scrub typhus infection using whole genome sequencing.
Ki-Woon Kang, et al. The Korean journal of internal medicine 2023 0 (6) 865-871 - Genome-Wide Association Study Identifies Eight Novel Loci for Susceptibility of Scrub Typhus and Highlights Immune-Related Signaling Pathways in Its Pathogenesis.
Kim Yong-Chan, et al. Cells 2021 3 (3) - Orientia tsutsugamushi DNA load and genotypes in blood as a marker of severity.
Kim Seok Won, et al. Acta tropica 2020 12 105786 - Clinical characteristics and risk factors of an outbreak with scrub typhus in previously unrecognized areas, Jiangsu province, China 2013.
Hu Jianli, et al. PloS one 2015 0 (5) e0125999 - Association between heat shock protein 70 gene polymorphisms and clinical outcomes in intensive care unit patients with sepsis.
Ramakrishna Kartik, et al. Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine 2014 4 (4) 205-11 - Single-nucleotide polymorphisms in Toll-like receptor (TLR)-2, TLR4 and heat shock protein 70 genes and susceptibility to scrub typhus.
Janardhanan Jeshina, et al. Journal of human genetics 2013 11 (11) 707-10 - Typhus
From NCATS Genetic and Rare Diseases Information Center
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 21, 2024
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