Home›Diseases of the Nervous System›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-attestedVI 1ICD-10 Code RangeWell-attestedG00-G99 1Genetic / HereditaryFilter Results88 entriesBody SystemAllEye (4)Integumentary System (1)Muscular System (14)Nervous System (72)ICD-10 ChapterAllIV: Endocrine, Nutritional and Metabolic Diseases (2)VI: Diseases of the Nervous System (64)VII: Diseases of the Eye and Adnexa (1)XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities (1)Communicable or Non-communicableAllNon-Communicable (79)Transmission RouteAllNon-Transmissible (31)Era (First Described)All1824 (2)1834 (1)1857 (1)1863 (1)1872 (1)1876 (1)1880 (1)1882 (1)1886 (1)1890 (1)1891 (2)1897 (1)1902 (1)1909 (1)1911 (1)1930 (1)1935 (1)1936 (1)1937 (1)1940 (1)1943 (1)1951 (1)1952 (1)1956 (1)1963 (1)1964 (1)1971 (2)1976 (1)1978 (1)1979 (1)1984 (1)1987 (1)1988 (1)1994 (1)1998 (1)2014 (1)Treated ByAllAnimal-Assisted Therapy (1)Applied Behavior Analysis (1)Bacteriotherapy (1)Equine-Assisted Therapy (1)Fetal Tissue Implant (1)Hippotherapy (1)Intracerebroventricular Injection (1)Neurofeedback (1)Physical Therapy (2)Play Therapy (1)Psychoanalysis (1)Rebirthing Therapy (1)Speech-Language Pathology (1)DiscovererAllJean-Martin Charcot (1)Show ResultsBrowseCompareSelect all 38Leigh syndromeGenetic / HereditaryMachado-Joseph diseaseGenetic / HereditaryMarinesco-Sjögren syndromeGenetic / HereditaryMELAS SyndromeGenetic / HereditaryMetachromatic leukodystrophyGenetic / HereditaryMuscle-eye-brain diseaseGenetic / HereditaryMyoclonic dystoniaGenetic / HereditaryMyotonia congenitaGenetic / HereditaryMyotonic dystrophyGenetic / HereditaryNemaline myopathyGenetic / HereditaryNeuroacanthocytosisGenetic / HereditaryNeuroferritinopathyGenetic / HereditaryNeurofibromatosisGenetic / HereditaryPantothenate kinase-associated neurodegenerationGenetic / HereditaryParamyotonia congenitaGenetic / HereditaryParoxysmal extreme pain disorderGenetic / HereditaryParoxysmal kinesigenic dyskinesiaGenetic / HereditaryPelizaeus-Merzbacher diseaseGenetic / HereditaryPeriodic paralysisGenetic / HereditaryPrimary familial brain calcificationGenetic / HereditaryProgressive myoclonus epilepsyGenetic / HereditaryPURA syndromeGenetic / HereditaryRefsum diseaseGenetic / HereditarySalt and pepper syndromeGenetic / HereditarySLC6A1 epileptic encephalopathyGenetic / HereditarySpastic paraplegia 31Genetic / HereditarySpinal and bulbar muscular atrophyGenetic / HereditarySpinal Muscular AtrophyGenetic / HereditarySpinal muscular atrophy with progressive myoclonic epilepsyGenetic / HereditarySpinocerebellar ataxia type 1Genetic / HereditarySpinocerebellar ataxia type 13Genetic / HereditarySpinocerebellar ataxia type 2Genetic / HereditarySpinocerebellar ataxia type 6Genetic / HereditarySpinocerebellar ataxia type 7Genetic / HereditaryUllrich congenital muscular dystrophyGenetic / HereditaryUnverricht-Lundborg diseaseGenetic / HereditaryXia-Gibbs syndromeGenetic / HereditaryX-linked dystonia parkinsonismGenetic / HereditaryShowing 51 to 88 of 88, page 2 of 2.← Previous12Sources1. ICD-10 (Wikipedia)ICD-10 chapter table, Chapter VI, chapter numberVI | G00-G99 | "Diseases of the nervous system"ICD-10 chapter table, Chapter VI, code rangeVI | G00-G99 | "Diseases of the nervous system"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.