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Results 1 - 10 of 39 for Leukocyte disorder
  1. Leukocyte adhesion deficiency type 1 
    Leukocyte adhesion deficiency type 1 is a disorder that causes the immune system to malfunction, resulting in a form of immunodeficiency. Immunodeficiencies are conditions ...
    https://medlineplus.gov/.../leukocyte-adhesion-deficiency-type-1 - Genetics
  2. MYH9-related disorder 
    ... cells such as platelets and white blood cells (leukocytes) use only myosin IIA.MYH9 gene mutations that cause MYH9-related disorder typically result in a nonfunctional version of the ...
    https://medlineplus.gov/genetics/condition/myh9-related-disorder - Genetics
  3. 8p11 myeloproliferative syndrome 
    ... by a high number of white blood cells (leukocytes). Most affected individuals also have an excess of myeloid cells known as eosinophils (eosinophilia).In addition to a myeloproliferative disorder, many people with 8p11 myeloproliferative syndrome develop lymphoma, ...
    https://medlineplus.gov/.../8p11-myeloproliferative-syndrome - Genetics
  4. Chediak-Higashi syndrome 
    ... Chediak-Steinbrinck-Higashi syndrome CHS Oculocutaneous albinism with leukocyte defect Genetic Testing Registry: Chédiak-Higashi syndrome Chédiak-Higashi syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov CHEDIAK-HIGASHI SYNDROME; CHS PubMed ...
    https://medlineplus.gov/genetics/condition/chediak-higashi-syndrome - Genetics
  5. Paroxysmal nocturnal hemoglobinuria 
    ... death and impaired production of blood cells. The disorder affects red blood cells (erythrocytes), which carry oxygen; white blood cells (leukocytes), which protect the body from infections; and platelets ( ...
    https://medlineplus.gov/.../paroxysmal-nocturnal-hemoglobinuria - Genetics
  6. Bare lymphocyte syndrome type II 
    ... combined immunodeficiency due to absent class II human leukocyte antigens Severe combined immunodeficiency, HLA class II-negative ... BARE LYMPHOCYTE SYNDROME, TYPE II ...
    https://medlineplus.gov/.../bare-lymphocyte-syndrome-type-ii - Genetics
  7. Type 1 diabetes 
    ... to a family of genes called the human leukocyte antigen (HLA) complex. The HLA ... disorder. Autoimmune disorders occur when the immune system attacks ...
    https://medlineplus.gov/genetics/condition/type-1-diabetes - Genetics
  8. Chanarin-Dorfman syndrome 
    ... Chanarin disease Dorfman-Chanarin syndrome Ichthyosiform Erythroderma with Leukocyte Vacuolation Ichthyotic neutral lipid storage disease Neutral lipid ... PubMed ...
    https://medlineplus.gov/genetics/condition/chanarin-dorfman-syndrome - Genetics
  9. Autoimmune Addison disease 
    ... Addison disease Addison disease National Organization for Rare Disorders (NORD) PubMed Gombos Z, Hermann R, Kiviniemi M, Nejentsev S, Reimand K, Fadeyev V, Peterson P, Uibo R, Ilonen J. Analysis of extended human leukocyte antigen haplotype association with Addison's disease in ...
    https://medlineplus.gov/.../condition/autoimmune-addison-disease - Genetics
  10. Ankylosing spondylitis 
    ... genes that influence the risk of developing this disorder.The HLA-B gene provides instructions for making a protein that plays an important role in the immune system. The HLA-B gene is part of a family of genes called the human leukocyte antigen (HLA) complex. The HLA complex helps the ...
    https://medlineplus.gov/genetics/condition/ankylosing-spondylitis - Genetics
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