Synovitis
What's New
Last Posted: Nov 04, 2021
- The Assessment of Selected miRNA Profile in Familial Mediterranean Fever.
Kahraman Cigdem Yuce et al. BioMed research international 2021 20216495700 - Classifying Pseudogout using Machine Learning Approaches with Electronic Health Record Data.
Tedeschi Sara K et al. Arthritis care & research 2020 Jan - Familial Mediterranean Fever: Assessing the Overall Clinical Impact and Formulating Treatment Plans.
Manna Raffaele et al. Mediterranean journal of hematology and infectious diseases 2019 11(1) e2019027 - Neural networks for automatic scoring of arthritis disease activity on ultrasound images.
Andersen Jakob Kristian Holm et al. RMD open 2019 5(1) e000891 - CLINGEN Actionability Report for Familial Mediterranean Fever (AD) - MEFV
ClinGen Actionability Working Group - CLINGEN Actionability Report for Familial Mediterranean Fever (AR) - MEFV
ClinGen Actionability Working Group - Review - Rheumatoid arthritis: What have we learned about the causing factors?
Jalil Syed Fazal et al. Pakistan journal of pharmaceutical sciences 2016 Mar 29(2) 629-45 - Pigmented villonodular synovitis
From NCATS Genetic and Rare Diseases Information Center - Synovitis
From NCATS Genetic and Rare Diseases Information Center - Talo-patello-scaphoid osteolysis, synovitis, and short fourth metacarpals
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 25, 2024
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