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 50Lymphedema-Distichiasis SyndromeGenetic / HereditaryMacrocephaly-capillary malformationGenetic / HereditaryMajewski's polydactyly syndromeGenetic / HereditaryMalouf syndromeGenetic / HereditaryMalpuech Facial Clefting SyndromeGenetic / HereditaryMandibulofacial dysostosis-microcephaly syndromeGenetic / HereditaryMarden-Walker syndromeGenetic / HereditaryMarfan SyndromeGenetic / HereditaryMarshall syndromeGenetic / HereditaryMcCune-Albright SyndromeGenetic / HereditaryMcKusick-Kaufman syndromeGenetic / HereditaryMECP2 duplication syndromeGenetic / HereditaryMEDNIK syndromeGenetic / HereditaryMegalocorneaGenetic / HereditaryMelnick-Needles syndromeGenetic / HereditaryMicrocephalic osteodysplastic primordial dwarfism type IIGenetic / HereditaryMicrocephalyGenetic / HereditaryMicrocephaly lymphoedema chorioretinal dysplasiaGenetic / HereditaryMicrodeletion syndromeGenetic / HereditaryMicrohydranencephalyGenetic / HereditaryMicromastiaGenetic / HereditaryMicrophthalmia-dermal aplasia-sclerocornea syndromeGenetic / HereditaryMiller syndromeGenetic / HereditaryMiller-Dieker syndromeGenetic / HereditaryMOMO syndromeGenetic / HereditaryMowat-Wilson syndromeGenetic / HereditaryMuenke syndromeGenetic / HereditaryMulibrey nanismGenetic / HereditaryMultiple epiphyseal dysplasiaGenetic / HereditaryMuscular DystrophyGenetic / HereditaryMyhre syndromeGenetic / HereditaryNager acrofacial dysostosisGenetic / HereditaryNail-patella syndromeGenetic / HereditaryNeurofibromatosis Type 1Genetic / HereditaryNicolaides-Baraitser syndromeGenetic / HereditaryNijmegen breakage syndromeGenetic / HereditaryNoonan SyndromeGenetic / HereditaryNoonan syndrome with multiple lentiginesGenetic / HereditaryOpitz G/BBB syndromeGenetic / HereditaryOrofaciodigital syndrome 1Genetic / HereditaryOsteogenesis ImperfectaGenetic / HereditaryOsteopetrosisGenetic / HereditaryPallister-Hall syndromeGenetic / HereditaryPallister-Killian syndromeGenetic / HereditaryPascual-Castroviejo syndrome type 1Genetic / HereditaryPatau SyndromeGenetic / HereditaryPentasomy XGenetic / HereditaryPerlman syndromeGenetic / HereditaryPersistent Müllerian duct syndromeGenetic / HereditaryPeters-plus syndromeGenetic / HereditaryShowing 151 to 200 of 278, page 4 of 6.← Previous123456Next →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.