Create issue ticket

385 Possible Causes for Heinz Body Anemia

  • Congenital Heinz Body Hemolytic Anemia

    CHBHA stands for "Congenital Heinz Body Hemolytic Anemia" How to abbreviate Congenital Heinz Body Hemolytic Anemia?[allacronyms.com] Abstract The mechanisms of hemoglobin precipitation into Heinz bodies and hemolytic anemia that characterize congenital Heinz body hemolytic anemia (CHBHA) were studied in[ncbi.nlm.nih.gov] One of the meanings of CHBHA is "Congenital Heinz Body Hemolytic Anemia" What is the abbreviation for Congenital Heinz Body Hemolytic Anemia?[allacronyms.com]

  • Heinz Body Anemia

    body anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.[amp.pharm.mssm.edu] […] hemoglobin, found on the membrane of red blood cells. ( Human Phenotype Ontology , HP_0005511 ) External Link Similar Terms Downloads & Tools Genes 2 genes associated with the heinz[amp.pharm.mssm.edu] About a year after this treatment she developed a generalized weakness without renewal of the diarrhea; the diagnosis of Heinz body hemolytic anemia was established.[ncbi.nlm.nih.gov]

  • Anemia

    Heinz bodies form in the cytoplasm of RBCs and appear as small dark dots under the microscope. In animals, Heinz body anemia has many causes.[en.wikipedia.org] […] when exposed to oxidative stress Low enzyme activity; with hemolysis smear may show poikilocytosis, reticulocytosis, Heinz bodies, and bite cells (in G6PD deficiency) or[aafp.org] Evidence for multiple causes appears with an elevated RBC distribution width (RDW), indicating a wider-than-normal range of red cell sizes, also seen in common nutritional anemia[en.wikipedia.org]

  • Hemoglobinopathy

    body anemia Acquired hemoglobinopathy Arthropathy secondary to hemoglobinopathy Decreased erythrocyte life span Double heterozygous sickling disorder Heinz bodies Hematopoietic[icd9data.com] […] cell destruction finding Sickle cell retinopathy Thalassemia-hemoglobin C disease Unstable hemoglobin disease 282.7 Excludes Applies To Abnormal hemoglobin NOS Congenital Heinz-body[icd9data.com] Applicable To Abnormal hemoglobin NOS Congenital Heinz body anemia Hb-C disease Hb-D disease Hb-E disease Hemoglobinopathy NOS Unstable hemoglobin hemolytic disease Type 1[icd10data.com]

  • Uremic Pneumonitis

    In further assessing the etiology of this massive hemolytic anemia, a peripheral blood smear revealed no Heinz bodies and a mixed picture of spherocytes and microangiopathic[pedsccm.org]

  • Hereditary Spherocytosis

    Assessment of red cell morphology and normal test results allowed diagnosis of infantile pyknocytosis or Heinz body anemia in three neonates.[ncbi.nlm.nih.gov] Such patients usually have a positive Heinz-body stain.[healio.com] Rarely, spherocytic hemolytic anemia may be the only initial manifestation of Wilson's disease.5 Another diagnostic difficulty is caused by patients with HS who present during[healio.com]

  • Dilated Cardiomyopathy 1R

    body anemias Hemoglobin H disease Hereditary angioneurotic edema Hereditary diffuse gastric cancer Hereditary factor IX deficiency disease Hereditary factor VIII deficiency[pentacorelab.hu] body anemia 140700 HBA2 hemoglobin, alpha 2 Enf-389 Heinz body anemias, beta- 140700 HBB hemoglobin, beta Enf-390 Hemangioblastoma, cerebellar, somatic VHL von Hippel-Lindau[ac-gen.com] […] disease type 4 Gorlin syndrome Grebe syndrome Growth mental deficiency syndrome of Myhre Guillain-Barre syndrome, familial Hb SS disease Heart-hand syndrome, Slovenian type Heinz[pentacorelab.hu]

  • Waisman Syndrome

    141749 Erythremias, beta- 141800 Heinz body anemias, beta- 140700 Hereditary persistence of fetal hemoglobin 141749 Methemoglobinemias, beta- 141900 Sickle cell anemia 603903[institutobernabeu.com] body anemias, alpha- 140700 Hemoglobin H disease, nondeletional 613978 Methemoglobinemias, alpha- 141800 Thalassemias, alpha- 604131 H B B 11p15.4 Delta-beta thalassemia[institutobernabeu.com] 609015 HA M P 19q13.12 Hemochromatosis, type 2B 613313 HA X1 1q21.3 Neutropenia, severe congenital 3, autosomal recessive 610738 H B A 1 16p13.3 Erythremias, alpha- 141800 Heinz[institutobernabeu.com]

  • Posthemorrhagic Anaemia of the Newborn

    […] additional code for type of crisis, such as: Acute chest syndrome (517.3) Splenic sequestration (289.52) 282.7 Other hemoglobinopathies Abnormal hemoglobin NOS Congenital Heinz-body[theodora.com] body anemia Hb-C disease Hb D disease Hb-E disease Hemoglobinopathy NOS Unstable hemoglobin hemolytic disease Excludes1: familial polycythemia (D75.0) Hb-M disease (D74.0[en.wikisource.org] anemia Disease: hemoglobin C [Hb-C] hemoglobin D [Hb-D] hemoglobin E [Hb-E] hemoglobin Zurich [Hb-Zurich] Hemoglobinopathy NOS Hereditary persistence of fetal hemoglobin[theodora.com]

  • Sick Sinus Syndrome

    body anemias Hemoglobin H disease Hereditary angioneurotic edema Hereditary diffuse gastric cancer Hereditary factor IX deficiency disease Hereditary factor VIII deficiency[pentacorelab.hu] […] disease type 4 Gorlin syndrome Grebe syndrome Growth mental deficiency syndrome of Myhre Guillain-Barre syndrome, familial Hb SS disease Heart-hand syndrome, Slovenian type Heinz[pentacorelab.hu]

Further symptoms