Last Posted: Jan 21, 2021
- Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes.
Cerqueira Juliana X M, et al. Journal of human genetics 2021 1
- Symptoms & Causes of Celiac Disease
Research suggests that celiac disease happens to individuals who have particular genes carried by about one-third of the population. NIDDK 2018
- The HLA Alleles B*0801 and DRB1*0301 Are Associated with Dermatitis Herpetiformis in a Chinese Population.
Sun Yonghu, et al. The Journal of investigative dermatology 2016 2 (2) 530-2
- Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.
Garner Chad, et al. PloS one 2014 0 (7) e101428
- Genetic polymorphisms of CYP2D6 oxidation in patients with autoimmune bullous diseases.
Rychlik-Sych Mariola, et al. Post?py dermatologii i alergologii 2013 8 (4) 211-7
- Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population.
Parmar AS, et al. Tissue antigens 2012 10
- Dermatitis herpetiformis
From NCATS Genetic and Rare Diseases Information Center
- Increased frequency of Ig heavy-chain HS1,2-A enhancer *2 allele in dermatitis herpetiformis, plaque psoriasis, and psoriatic arthritis.
Cianci Rossella, et al. The Journal of investigative dermatology 2008 8 (8) 1920-4
- Haptoglobin polymorphism: a novel genetic risk factor for celiac disease development and its clinical manifestations.
Papp Maria, et al. Clinical chemistry 2008 4 (4) 697-704
- Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association.
Koskinen L L E, et al. Journal of medical genetics 2008 4 (4) 222-7
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.