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 40Lysinuric protein intoleranceRare (Under 1 in 2000)Maple Syrup Urine DiseaseRare (Under 1 in 2000)MDP syndromeRare (Under 1 in 2000)Medium-chain acyl-coenzyme A dehydrogenase deficiencyRare (Under 1 in 2000)Menkes diseaseRare (Under 1 in 2000)MEPAN syndromeRare (Under 1 in 2000)Mevalonate kinase deficiencyRare (Under 1 in 2000)Mucolipidosis type IVRare (Under 1 in 2000)Mucopolysaccharidosis type IRare (Under 1 in 2000)Multiple endocrine neoplasia type 1Rare (Under 1 in 2000)Multiple endocrine neoplasia type 2Rare (Under 1 in 2000)Multiple sulfatase deficiencyRare (Under 1 in 2000)Neutral lipid storage diseaseRare (Under 1 in 2000)Niemann-Pick disease type CRare (Under 1 in 2000)Occipital horn syndromeRare (Under 1 in 2000)Oculocutaneous albinismRare (Under 1 in 2000)Ornithine transcarbamylase deficiencyRare (Under 1 in 2000)Pendred syndromeRare (Under 1 in 2000)PorphyriaRare (Under 1 in 2000)Propionic acidemiaRare (Under 1 in 2000)Pyruvate dehydrogenase deficiencyRare (Under 1 in 2000)Rabson-Mendenhall syndromeRare (Under 1 in 2000)ROHHADRare (Under 1 in 2000)Rotor syndromeRare (Under 1 in 2000)Salla diseaseRare (Under 1 in 2000)Sandhoff diseaseRare (Under 1 in 2000)Sanfilippo syndromeRare (Under 1 in 2000)Schindler diseaseRare (Under 1 in 2000)SitosterolemiaRare (Under 1 in 2000)Smith-Lemli-Opitz syndromeRare (Under 1 in 2000)Succinic semialdehyde dehydrogenase deficiencyRare (Under 1 in 2000)Succinyl-CoA:3-oxoacid CoA transferase deficiencyRare (Under 1 in 2000)Tangier diseaseRare (Under 1 in 2000)Transaldolase deficiencyRare (Under 1 in 2000)Tyrosinemia type IRare (Under 1 in 2000)Urbach-Wiethe diseaseRare (Under 1 in 2000)Werner syndromeRare (Under 1 in 2000)Wolfram syndromeRare (Under 1 in 2000)X-linked adrenal hypoplasia congenitaRare (Under 1 in 2000)Zellweger syndromeRare (Under 1 in 2000)Showing 51 to 90 of 90, page 2 of 2.← Previous12Sources1. 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.