Severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive
Other Names for this Disease
- SCID due to artemis deficiency
- SCID due to DCLRE1C deficiency
- SCID, AR, T-cell negative, B-cell negative, NK cell-positive
- SCID, Athabascan type
- SCID, Athabaskan type
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.
These Web pages are updated as the Genetic and Rare Diseases Information Center receives questions and as new information becomes available. If you don’t see many information resources on this page, it may be because the Information Center hasn’t yet received a question about this condition.
Your Questions Answeredby the Genetic and Rare Diseases Information Center
Please contact us with your questions about Severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive. We will answer your question and update these pages with new resources and information.
- Genetics Home Reference (GHR) contains information on Severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive. This website is maintained by the National Library of Medicine.
- The National Human Genome Research Institute's (NHGRI) mission encompasses a broad range of studies aimed at understanding the structure and function of the human genome and its role in health and disease. Click on the link to view the information page on this topic.
- The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- Zhang,et al. Novel RAG1 Mutation in a Case of Severe Combined Immunodeficiency. Pediatrics 2005;116: e445-e449.