Last Posted: Feb 22, 2021
- HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study.
Koskela Mikael, et al. Pediatric nephrology (Berlin, Germany) 2021 2
- The Role of MIF-173G/C Gene Polymorphism in the Susceptibility of Autoimmune Diseases.
Du Xiangrong, et al. Mediators of inflammation 2020 0 7825072
- Familial Mediterranean fever is associated with a wide spectrum of inflammatory disorders: results from a large cohort study.
Atas Nuh, et al. Rheumatology international 2019 8
- The Influence of Concomitant Disorders on Disease Severity of Familial Mediterranean Fever in Children.
Kisla Ekinci Rabia Miray, et al. Archives of rheumatology 2018 9 (3) 282-287
- MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience.
Ekinci Rabia Miray Kisla, et al. Postgraduate medicine 2019 1 (1) 68-72
- Lack of Association between Interleukin-8 Gene +781 C/T Polymorphism and Henoch-Schönlein Purpura in Childhood.
Xu Hui, et al. Iranian journal of allergy, asthma, and immunology 2016 6 (3) 237-43
- Association between IL17A and IL17F polymorphisms and risk of Henoch-Schonlein purpura in Chinese children.
Xu Hui, et al. Rheumatology international 2016 6 (6) 829-35
- Interleukin 1 beta (IL1ß) rs16944 genetic variant as a genetic marker of severe renal manifestations and renal sequelae in Henoch-Schönlein purpura.
López-Mejías Raquel, et al. Clinical and experimental rheumatology 0 0 (3 Suppl 97) S84-8
- Angiotensin-converting enzyme insertion/deletion polymorphism and susceptibility to Henoch-Schönlein purpura: a meta-analysis.
Zhang Xiaoqing, et al. Journal of the renin-angiotensin-aldosterone system : JRAAS 0 0 (1) 1470320319836302
- MEFV gene variants in children with Henoch-Schönlein Purpura and association with clinical manifestations: a single center Mediterranean experience.
Ekinci Rabia Miray Kisla et al. Postgraduate medicine 2018 Dec
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
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Graves Disease
- Huntington Disease
- Myasthenia Gravis
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics 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.