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Results 1 - 10 of 12 for Anemia due to chronic disorder
  1. Glucose phosphate isomerase deficiency 
    ... deficiency Glucosephosphate isomerase deficiency ... of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemia. Blood. 1996 Sep 15;88(6): ...
    https://medlineplus.gov/.../glucose-phosphate-isomerase-deficiency - Genetics
  2. 5q minus syndrome 
    ... Myelodysplastic syndrome with 5q deletion syndrome Refractory macrocytic anemia due to 5q deletion Genetic Testing Registry: Myelodysplastic syndrome ...
    https://medlineplus.gov/genetics/condition/5q-minus-syndrome - Genetics
  3. Pyruvate kinase deficiency 
    ... Registry: Pyruvate kinase deficiency of red cells Hemolytic anemia due to red cell pyruvate kinase deficiency National Organization ...
    https://medlineplus.gov/.../condition/pyruvate-kinase-deficiency - Genetics
  4. Spondyloenchondrodysplasia with immune dysregulation 
    ... thrombocytopenia), premature destruction of red blood cells (hemolytic anemia), an underactive thyroid gland (hypothyroidism), or chronic inflammatory disorders such as systemic lupus erythematosus or rheumatoid arthritis. ...
    https://medlineplus.gov/...hondrodysplasia-with-immune-dysregulation - Genetics
  5. Ulcerative colitis 
    ... loss of appetite, bowel urgency, fatigue, and fevers. Chronic bleeding from the inflamed and ulcerated intestinal tissue can cause a shortage of red blood cells (anemia) in some affected individuals. People with this disorder have difficulty absorbing enough fluids and nutrients from ...
    https://medlineplus.gov/genetics/condition/ulcerative-colitis - Genetics
  6. STAT3 gene 
    ... autoimmune disorder, primarily rheumatoid arthritis or autoimmune hemolytic ... lymphoproliferative disorders of NK cells (CLPD-NKs). Both forms have ...
    https://medlineplus.gov/genetics/gene/stat3 - Genetics
  7. Nakajo-Nishimura syndrome 
    ... conditions: one called joint contractures, muscular atrophy, microcytic ... considered separate disorders, they are caused by mutations in the same ...
    https://medlineplus.gov/genetics/condition/nakajo-nishimura-syndrome - Genetics
  8. PSMB8 gene 
    ... above): one called joint contractures, muscular atrophy, microcytic anemia, ... disorders, some researchers believe they may represent different forms ...
    https://medlineplus.gov/genetics/gene/psmb8 -
  9. Phosphoglycerate kinase deficiency 
    ... some features of phosphoglycerate kinase deficiency, such as anemia. A characteristic of X-linked inheritance is that fathers cannot ... kinase 1 deficiency Glycogen storage disease ...
    https://medlineplus.gov/.../phosphoglycerate-kinase-deficiency - Genetics
  10. Crohn's disease 
    Crohn's disease is a complex, long-lasting (chronic) disorder that primarily affects the digestive system. This condition ... to a low number of red blood cells (anemia). In some cases, Crohn's disease can also ...
    https://medlineplus.gov/genetics/condition/crohns-disease - Genetics
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