Home›Endocrine, Nutritional and Metabolic Diseases›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-attestedIV 1ICD-10 Code RangeWell-attestedE00-E90 1Rare (Under 1 in 2000)Filter Results90 entriesBody SystemAllCardiovascular System (2)Digestive System (6)Ear (2)Endocrine System (22)Eye (5)Integumentary System (5)Lymphatic or Immune System (1)Muscular System (3)Nervous System (21)Skeletal System (4)Urinary System (6)ICD-10 ChapterAllIV: Endocrine, Nutritional and Metabolic Diseases (70)XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities (1)Communicable or Non-communicableAllNon-Communicable (86)Causative AgentAllComplication of Another Disease (2)Genetic / Hereditary (88)Idiopathic / Multifactorial (1)Transmission RouteAllNon-Transmissible (33)Era (First Described)All-370 (1)1639 (1)1772 (1)1882 (1)1886 (1)1896 (1)1898 (1)1904 (1)1917 (2)1929 (2)1936 (1)1938 (1)1948 (1)1949 (1)1950 (1)1954 (2)1956 (1)1957 (1)1960 (1)1962 (1)1964 (1)1965 (1)1966 (1)1968 (1)1969 (1)1972 (1)1973 (1)1974 (2)1979 (1)1980 (1)1981 (2)2001 (1)2004 (1)2016 (1)Treated ByAllDialysis (1)Enzyme Replacement Therapy (1)Hematopoietic Stem Cell Transplantation (2)Occupational Therapy (1)Physical Therapy (2)Radiotherapy (1)Show ResultsBrowseCompareSelect all 50AbetalipoproteinemiaRare (Under 1 in 2000)AceruloplasminemiaRare (Under 1 in 2000)Acrodermatitis enteropathicaRare (Under 1 in 2000)AcromegalyRare (Under 1 in 2000)Adenine phosphoribosyltransferase deficiencyRare (Under 1 in 2000)Adenylosuccinate lyase deficiencyRare (Under 1 in 2000)Adult polyglucosan body diseaseRare (Under 1 in 2000)Alexander diseaseRare (Under 1 in 2000)ALG1-CDGRare (Under 1 in 2000)AlkaptonuriaRare (Under 1 in 2000)Alpha-mannosidosisRare (Under 1 in 2000)AmyloidosisRare (Under 1 in 2000)ArgininemiaRare (Under 1 in 2000)Argininosuccinic aciduriaRare (Under 1 in 2000)Aromatase deficiencyRare (Under 1 in 2000)Aromatase excess syndromeRare (Under 1 in 2000)AspartylglucosaminuriaRare (Under 1 in 2000)Bartter syndromeRare (Under 1 in 2000)Beta-ketothiolase deficiencyRare (Under 1 in 2000)Carbamoyl phosphate synthetase I deficiencyRare (Under 1 in 2000)Carnitine palmitoyltransferase II deficiencyRare (Under 1 in 2000)Cerebrotendinous xanthomatosisRare (Under 1 in 2000)Chylomicron retention diseaseRare (Under 1 in 2000)Congenital adrenal hyperplasiaRare (Under 1 in 2000)Congenital generalized lipodystrophyRare (Under 1 in 2000)Crigler-Najjar syndromeRare (Under 1 in 2000)CystinosisRare (Under 1 in 2000)Danon diseaseRare (Under 1 in 2000)Donohue syndromeRare (Under 1 in 2000)Fabry DiseaseRare (Under 1 in 2000)Familial Amyloidosis, Finnish TypeRare (Under 1 in 2000)Farber diseaseRare (Under 1 in 2000)Fumarase deficiencyRare (Under 1 in 2000)GalactosemiaRare (Under 1 in 2000)GalactosialidosisRare (Under 1 in 2000)Gaucher DiseaseRare (Under 1 in 2000)Glutaric aciduria type 1Rare (Under 1 in 2000)Glycogen storage disease type IRare (Under 1 in 2000)Glycogen storage disease type IVRare (Under 1 in 2000)Hartnup diseaseRare (Under 1 in 2000)Hereditary fructose intoleranceRare (Under 1 in 2000)Hermansky-Pudlak syndromeRare (Under 1 in 2000)Hunter syndromeRare (Under 1 in 2000)Hutchinson-Gilford Progeria SyndromeRare (Under 1 in 2000)HypophosphatasiaRare (Under 1 in 2000)Isovaleric acidemiaRare (Under 1 in 2000)Laron syndromeRare (Under 1 in 2000)Lecithin cholesterol acyltransferase deficiencyRare (Under 1 in 2000)Lesch-Nyhan syndromeRare (Under 1 in 2000)Leydig cell hypoplasiaRare (Under 1 in 2000)Showing 1 to 50 of 90, page 1 of 2.12Next →Sources1. ICD-10 (Wikipedia)ICD-10 chapter table, Chapter IV, chapter numberIV | E00-E90 | "Endocrine, nutritional and metabolic diseases"ICD-10 chapter table, Chapter IV, code rangeIV | E00-E90 | "Endocrine, nutritional and metabolic diseases"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.