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1,095 Possible Causes for Congenital Hemolytic Anemia, Non-Hemolytic Unconjugated Hyperbilirubinemia

  • Gilbert Syndrome

    Constitutional liver dysfunction Familial non-hemolytic non-obstructive jaundice Icterus intermittens juvenilis Low-grade chronic hyperbilirubinemia Unconjugated benign bilirubinemia[en.wikipedia.org] […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[icd10data.com] Tagged as: constitutional liver dysfunction, familial benign unconjugated hyperbilirubinaemia, familial non-hemolytic non-obstructive jaundice, Gilbert–Meulengracht syndrome[highrisklifeinsuranceagency.com]

  • Pyruvate Kinase Deficiency

    It constitutes one of the common causes of hereditary non-spherocytic hemolytic anemia.[ncbi.nlm.nih.gov] HEREDITARY spherocytosis with its associated congenital hemolytic anemia is generally easily recognized and satisfactorily treated with splenectomy.[nejm.org] Pyruvate kinase deficiency is a rare cause of congenital hemolytic anemia.[ncbi.nlm.nih.gov]

  • Crigler-Najjar Syndrome Type 1

    Mutations in the UGT1A1 gene cause Crigler-Najjar syndrome (CN), which causes non-hemolytic unconjugated hyperbilirubinemia, and is categorized as CN1 and CN2 according to[ncbi.nlm.nih.gov] […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[icd10data.com] Crigler-Najjar (CN) syndrome is a rare autosomal recessive inherited disorder characterized by non-hemolytic, unconjugated hyperbilirubinemia.[ncbi.nlm.nih.gov]

  • Hereditary Spherocytosis

    […] biconcave disk shape Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia edit English hereditary spherocytosis congenital hemolytic anemia[wikidata.org] Abstract Hereditary spherocytosis (HS) is a disease affecting the red blood cells membrane and belongs to the congenital hemolytic anemias.[ncbi.nlm.nih.gov] From Wikidata Jump to navigation Jump to search congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal[wikidata.org]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Hemoglobinopathy

    BACKGROUND: Hemoglobinopathies are a very heterogeneous group of congenital hemolytic anemia.[ncbi.nlm.nih.gov] […] persistence of fetal hemoglobin) ("Swiss variety") 282.7 unstable hemoglobin hemolytic 282.7 Elliptocytosis (congenital) (hereditary) 282.1 Hb-C (disease) 282.7 hemoglobin[icd9data.com] Anomaly hemoglobin (see also Disease, hemoglobin) 282.7 Anemia 285.9 Heinz-body, congenital 282.7 Disease, diseased - see also Syndrome hemoglobin (Hb) 282.7 HPFH (hereditary[icd9data.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Erythrocyte Membrane Abnormality

    .: Congenital hemolytic anemia with high-sodium, low-potassium red cells. New Engl. J. Med. 280 , 909 (1969) PubMed Google Scholar 18.[link.springer.com] […] support Publication types Research Support, N.I.H., Extramural Review MeSH terms Anemia, Hemolytic, Congenital/blood* Anemia, Hemolytic, Congenital/complications Anemia,[ncbi.nlm.nih.gov] […] ulcerative colitis Hemolytic anemia, hereditary Hemolytic anemia, lymphoproliferative disease Hemolytic anemia, with ulcerative colitis Hereditary hemolytic anemia Clinical[icd10data.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Autoimmune Hemolytic Anemia

    […] from congenital hemolytic anemia.[en.wikipedia.org] Causes of and Risk Factors for Hemolytic Anemia There are two major types of hemolytic anemia: Congenital hemolytic anemia is a condition in which red blood cells die off[everydayhealth.com] Enzyme Deficiency Congenital Hemolytic Anemias: G6PD deficiency, pyruvate kinase deficiency, and others AIHA could be confused with a hemolytic crisis in patients with G-6[oncologynurseadvisor.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Cooley's Anemia

    , Hemolytic, Congenital Anemia, Hemolytic Hemoglobinopathies Genetic Diseases, Inborn Iron Metabolism Disorders Lung Diseases Respiratory Tract Diseases Sildenafil Citrate[clinicaltrials.gov] Thalassemia Iron Overload Hematologic Diseases beta-Thalassemia Hypertension, Pulmonary Bone Diseases, Metabolic Bone Diseases Musculoskeletal Diseases Metabolic Diseases Anemia[clinicaltrials.gov] Publications: Keywords provided by New England Research Institutes: chelator iron transfusion anemia thalassemia Additional relevant MeSH terms: Layout table for MeSH terms Anemia[clinicaltrials.gov]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Hemolytic Anemia

    A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.[icd9data.com] Congenital Hemolytic Anemia In congenital hemolytic anemias, the destruction of red blood cells is caused by a defect within the red blood cells themselves.[ucsfbenioffchildrens.org] Congenital hemolytic anemias are present at birth and may or may not be inherited.[innvista.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Glycogen Storage Disease Type 1

    Pyrimidine 5' nucleotidase deficiency presents with congenital hemolytic anemia because the residual nucleotides in young red cells (reticulocytes) cannot be metabolized and[cancertherapyadvisor.com] […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[icd10data.com] Pyruvate kinase deficiency is the most common glycolytic enzyme deficiency that leads to life-long hemolytic anemia.[cancertherapyadvisor.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia

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