Home›Diseases of the Blood and Immune Mechanism›Causative Agent›Genetic / HereditaryBrowse ByGenetic / HereditaryThis dimension names the agent that actually causes a medical condition, a pathogen, a genetic mutation or an environmental factor. Wikipedia notes that "a disease may be caused by external factors such as pathogens or by internal dysfunctions." Browsing this way collects every condition caused by the same agent.FactsGenetic / HereditarySourcesComments (0)Reader Challenges (0)FactsComparisonICD-10 Chapter NumberWell-attestedIII 1ICD-10 Code RangeWell-attestedD50-D89 1Genetic / HereditaryFilter Results77 entriesBody SystemAllCardiovascular System (1)Ear (2)Endocrine System (1)Eye (1)Integumentary System (2)Lymphatic or Immune System (52)Nervous System (1)Skeletal System (1)Urinary System (1)ICD-10 ChapterAllIII: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism (56)IV: Endocrine, Nutritional and Metabolic Diseases (1)XIII: Diseases of the Musculoskeletal System and Connective Tissue (1)Communicable or Non-communicableAllNon-Communicable (66)Transmission RouteAllNon-Transmissible (43)Era (First Described)All1871 (1)1881 (1)1926 (1)1938 (1)1951 (1)1952 (1)1953 (1)1954 (2)1955 (1)1956 (1)1961 (2)1965 (2)1968 (1)1969 (1)1972 (1)1975 (2)1978 (1)1979 (1)1981 (1)1994 (1)2004 (1)2010 (1)2011 (1)2012 (2)Treated ByAllAntifungal Therapy (1)Blood Donation (1)Bone Marrow Transplantation (3)Cord Blood Banking (1)Enzyme Replacement Therapy (1)Fresh Frozen Plasma Transfusion (1)Gene Therapy (1)Granulocyte colony-stimulating factor therapy (1)Granulocyte Transfusion (1)Hematopoietic Stem Cell Transplantation (1)Hyperimmune Globulin (1)Immunoglobulin Therapy (2)Insulin Therapy (1)Intrauterine Transfusion (1)Meningococcal Vaccine (1)Platelet Transfusion (2)Strimvelis (1)Thymus Transplantation (1)DiscovererAllOscar Ratnoff (1)Prevalence BandAllRare (Under 1 in 2000) (8)Show ResultsBrowseCompareSelect all 27Myeloperoxidase deficiencyGenetic / HereditaryNeutropeniaGenetic / HereditaryParoxysmal nocturnal hemoglobinuriaGenetic / HereditaryPASLI diseaseGenetic / HereditaryPelger-Huët anomalyGenetic / HereditaryPLAID syndromeGenetic / HereditaryPolycythemia VeraGenetic / HereditaryPrimary immunodeficiencyGenetic / HereditaryProperdin deficiencyGenetic / HereditaryProtein C deficiencyGenetic / HereditaryPurine nucleoside phosphorylase deficiencyGenetic / HereditaryPyruvate kinase deficiencyGenetic / HereditaryQuebec platelet disorderGenetic / HereditaryRh deficiency syndromeGenetic / HereditaryScott syndromeGenetic / HereditarySevere Combined ImmunodeficiencyGenetic / HereditarySevere congenital neutropeniaGenetic / HereditarySoutheast Asian ovalocytosisGenetic / HereditaryThiamine responsive megaloblastic anemia syndromeGenetic / HereditaryTNF receptor associated periodic syndromeGenetic / HereditaryVon Willebrand DiseaseGenetic / HereditaryWHIM syndromeGenetic / HereditaryWiskott-Aldrich SyndromeGenetic / HereditaryX-linked agammaglobulinemiaGenetic / HereditaryX-linked lymphoproliferative diseaseGenetic / HereditaryX-linked severe combined immunodeficiencyGenetic / HereditaryXMEN diseaseGenetic / HereditaryShowing 51 to 77 of 77, page 2 of 2.← Previous12Sources1. 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.