Home›Congenital Malformations and Chromosomal Abnormalities›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-attestedXVII 1ICD-10 Code RangeWell-attestedQ00-Q99 1Genetic / HereditaryFilter Results278 entriesBody SystemAllCardiovascular System (29)Digestive System (7)Ear (9)Endocrine System (7)Eye (22)Integumentary System (38)Lymphatic or Immune System (8)Muscular System (9)Nervous System (42)Reproductive System (10)Respiratory System (6)Skeletal System (72)Urinary System (13)ICD-10 ChapterAllIII: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism (1)IV: Endocrine, Nutritional and Metabolic Diseases (1)IX: Diseases of the Circulatory System (2)V: Mental and Behavioural Disorders (1)VI: Diseases of the Nervous System (2)XIII: Diseases of the Musculoskeletal System and Connective Tissue (1)XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities (194)Communicable or Non-communicableAllNon-Communicable (258)Transmission RouteAllNon-Transmissible (110)Era (First Described)All-400 (1)1575 (1)1657 (1)1691 (1)1803 (1)1817 (1)1833 (1)1848 (1)1851 (1)1862 (1)1866 (1)1869 (1)1874 (1)1879 (1)1880 (1)1881 (1)1886 (1)1889 (1)1896 (1)1900 (2)1903 (2)1904 (1)1906 (1)1909 (1)1910 (1)1912 (1)1919 (1)1928 (1)1929 (3)1932 (1)1933 (1)1934 (1)1935 (1)1936 (1)1937 (1)1938 (4)1942 (1)1943 (1)1950 (1)1951 (1)1952 (1)1954 (1)1955 (1)1956 (1)1957 (1)1959 (1)1960 (1)1961 (2)1962 (2)1963 (3)1964 (3)1965 (6)1966 (1)1969 (4)1970 (2)1971 (4)1972 (6)1973 (3)1974 (1)1975 (5)1976 (1)1977 (4)1979 (2)1980 (1)1981 (3)1982 (1)1983 (1)1984 (1)1985 (3)1986 (2)1987 (1)1988 (1)1989 (1)1991 (3)1992 (1)1993 (4)1997 (1)1998 (1)1999 (1)2000 (1)2002 (1)2003 (1)2005 (1)2006 (2)2007 (1)2013 (1)2014 (1)2015 (1)2021 (1)Treated ByAllAirway Clearance Therapy (1)Bentall Procedure (1)Bisphosphonate Therapy (1)Blood Transfusion (1)Cell Therapy (1)Chest Physiotherapy (1)Chest Wall Oscillation (2)Craniofacial Surgery (1)Cryoprecipitate Transfusion (1)Egg Donation (1)Exchange Transfusion (1)Fresh Frozen Plasma Transfusion (1)Gene Therapy (1)Hip Replacement Surgery (1)Hormone Therapy (1)Ileostomy (1)Nebulizer (1)Newborn Screening (1)Occupational Therapy (1)Palliative Care (1)Physical Therapy (4)Protein Replacement Therapy (1)Prothrombin Complex Concentrate (1)Rastelli Procedure (1)Speech-Language Therapy (1)Spinal Fusion (1)Splenectomy (1)DiscovererAllBert B. A. de Vries (1)David A. Koolen (1)Marco Fraccaro (1)Show ResultsBrowseCompareSelect all 501p36 deletion syndromeGenetic / Hereditary22q11.2 distal deletion syndromeGenetic / Hereditary22q13 deletion syndromeGenetic / Hereditary3C syndromeGenetic / Hereditary3-M syndromeGenetic / HereditaryAarskog-Scott syndromeGenetic / HereditaryAbruzzo-Erickson syndromeGenetic / HereditaryAcheiropodiaGenetic / HereditaryAchondrogenesisGenetic / HereditaryAchondroplasiaGenetic / HereditaryAcrodysostosisGenetic / HereditaryAcromicric dysplasiaGenetic / HereditaryAdams-Oliver syndromeGenetic / HereditaryADULT syndromeGenetic / HereditaryAicardi syndromeGenetic / HereditaryAlagille syndromeGenetic / HereditaryAllan-Herndon-Dudley syndromeGenetic / HereditaryAlport syndromeGenetic / HereditaryAlström syndromeGenetic / HereditaryAmish lethal microcephalyGenetic / HereditaryAndersen-Tawil syndromeGenetic / HereditaryAngelman SyndromeGenetic / HereditaryAniridiaGenetic / HereditaryAntley-Bixler syndromeGenetic / HereditaryApert syndromeGenetic / HereditaryArterial tortuosity syndromeGenetic / HereditaryArthrogryposis-renal dysfunction-cholestasis syndromeGenetic / HereditaryATR-X syndromeGenetic / HereditaryAutosomal dominant multiple pterygium syndromeGenetic / HereditaryAutosomal dominant polycystic kidney diseaseGenetic / HereditaryBainbridge-Ropers syndromeGenetic / HereditaryBaller-Gerold syndromeGenetic / HereditaryBarakat syndromeGenetic / HereditaryBarber-Say syndromeGenetic / HereditaryBardet-Biedl syndromeGenetic / HereditaryBerdon syndromeGenetic / HereditaryBilateral frontoparietal polymicrogyriaGenetic / HereditaryBjörnstad syndromeGenetic / HereditaryBloom syndromeGenetic / HereditaryBörjeson-Forssman-Lehmann syndromeGenetic / HereditaryBosch-Boonstra-Schaaf Optic Atrophy SyndromeGenetic / HereditaryBrachydactyly type DGenetic / HereditaryBranchio-oculo-facial syndromeGenetic / HereditaryBruck syndromeGenetic / HereditaryBurnside-Butler syndromeGenetic / HereditaryBuschke-Ollendorff SyndromeGenetic / HereditaryCampomelic dysplasiaGenetic / HereditaryCantú syndromeGenetic / HereditaryCardiofaciocutaneous syndromeGenetic / HereditaryCarpenter syndromeGenetic / HereditaryShowing 1 to 50 of 278, page 1 of 6.123…6Next →Sources1. ICD-10 (Wikipedia)ICD-10 chapter table, Chapter XVII, chapter numberXVII | Q00-Q99 | "Congenital malformations, deformations and chromosomal abnormalities"ICD-10 chapter table, Chapter XVII, code rangeXVII | Q00-Q99 | "Congenital malformations, deformations and chromosomal abnormalities"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.