Home›Diseases of the Blood and Immune Mechanism›Prevalence Band›Rare (Under 1 in 2000)Browse ByRare (Under 1 in 2000)FactsRare (Under 1 in 2000)SourcesComments (0)Reader Challenges (0)FactsComparisonICD-10 Chapter NumberWell-attestedIII 1ICD-10 Code RangeWell-attestedD50-D89 1Rare (Under 1 in 2000)Filter Results39 entriesBody SystemAllCardiovascular System (1)Ear (2)Endocrine System (1)Lymphatic or Immune System (30)Nervous System (1)Urinary System (1)ICD-10 ChapterAllII: Neoplasms (1)III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism (28)IV: Endocrine, Nutritional and Metabolic Diseases (1)XIII: Diseases of the Musculoskeletal System and Connective Tissue (1)Communicable or Non-communicableAllNon-Communicable (36)Causative AgentAllAutoimmune (6)Bacterial (1)Genetic / Hereditary (30)Idiopathic / Multifactorial (2)Transmission RouteAllNon-Transmissible (25)Era (First Described)All1753 (1)1871 (1)1881 (1)1924 (1)1926 (1)1938 (1)1952 (1)1954 (3)1955 (1)1956 (1)1959 (1)1961 (1)1968 (1)1969 (1)1972 (1)1975 (1)1978 (1)Treated ByAllCART4-34 therapy (1)Cord Blood Banking (1)Enzyme Replacement Therapy (1)Fresh Frozen Plasma Transfusion (1)Immunoglobulin Therapy (2)Immunosuppression (1)Immunosuppressive Therapy (1)Insulin Therapy (1)Pacing (Activity Management) (1)Platelet Transfusion (1)Strimvelis (1)Thymus Transplantation (1)DiscovererAllOscar Ratnoff (1)Show ResultsBrowseCompareSelect all 39Adenosine deaminase 2 deficiencyRare (Under 1 in 2000)AL amyloidosisRare (Under 1 in 2000)Antiphospholipid SyndromeRare (Under 1 in 2000)Atypical hemolytic uremic syndromeRare (Under 1 in 2000)Castleman diseaseRare (Under 1 in 2000)Chronic Granulomatous DiseaseRare (Under 1 in 2000)Congenital amegakaryocytic thrombocytopeniaRare (Under 1 in 2000)Congenital dyserythropoietic anemiaRare (Under 1 in 2000)Cyclic neutropeniaRare (Under 1 in 2000)Diamond-Blackfan anemiaRare (Under 1 in 2000)DiGeorge SyndromeRare (Under 1 in 2000)Epstein syndromeRare (Under 1 in 2000)Factor XII deficiencyRare (Under 1 in 2000)Fanconi anemiaRare (Under 1 in 2000)Granulomatosis with PolyangiitisRare (Under 1 in 2000)Griscelli syndrome type 2Rare (Under 1 in 2000)Hereditary elliptocytosisRare (Under 1 in 2000)Hereditary SpherocytosisRare (Under 1 in 2000)Hoyeraal-Hreidarsson syndromeRare (Under 1 in 2000)Hughes-Stovin SyndromeRare (Under 1 in 2000)Hypereosinophilic syndromeRare (Under 1 in 2000)Immunodeficiency-centromeric instability-facial anomalies syndromeRare (Under 1 in 2000)LIG4 syndromeRare (Under 1 in 2000)Muckle-Wells syndromeRare (Under 1 in 2000)Paroxysmal nocturnal hemoglobinuriaRare (Under 1 in 2000)Purine nucleoside phosphorylase deficiencyRare (Under 1 in 2000)Quebec platelet disorderRare (Under 1 in 2000)SclerodermaRare (Under 1 in 2000)Scott syndromeRare (Under 1 in 2000)Severe Combined ImmunodeficiencyRare (Under 1 in 2000)Severe congenital neutropeniaRare (Under 1 in 2000)Systemic Lupus ErythematosusRare (Under 1 in 2000)Thiamine responsive megaloblastic anemia syndromeRare (Under 1 in 2000)Thrombotic thrombocytopenic purpuraRare (Under 1 in 2000)Von Willebrand DiseaseRare (Under 1 in 2000)WHIM syndromeRare (Under 1 in 2000)Wiskott-Aldrich SyndromeRare (Under 1 in 2000)X-linked agammaglobulinemiaRare (Under 1 in 2000)X-linked lymphoproliferative diseaseRare (Under 1 in 2000)Sources1. ICD-10 (Wikipedia)ICD-10 chapter table, Chapter III, chapter numberIII | D50-D89 | "Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism"ICD-10 chapter table, Chapter III, code rangeIII | D50-D89 | "Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism"Comments (0)No comments yet. Be the first to share a thought.Sign in to join the discussion.Reader Challenges (0)No disputes yet. Spotted an error or a better source? Open the first one.Sign in to dispute this or suggest a correction.