{"orpha":91088,"name":"Other metabolic disease","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-91088/","orphanet_url":"https://www.orpha.net/en/disease/detail/91088","names":{"fr":{"name":"Autre maladie métabolique"},"de":{"name":"Stoffwechselstörung, sonstige"},"es":{"name":"Otra enfermedad metabólica"},"it":{"name":"Altra malattia metabolica"},"nl":{"name":"Andere stofwisselingsziekte"},"pt":{"name":"Outra doença metabólica"},"pl":{"name":"Inne choroby metaboliczne"},"cs":{"name":"Jiná metabolická porucha"},"uk":{"name":"Інші метаболічні захворювання"},"zh":{"name":"其他代谢性疾病"},"tr":{"name":"Diğer metabolik hastalık"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":68367,"name":"Rare inborn error of metabolism","classifications":[150,156]}],"children":[{"orpha":404454,"name":"Alacrimia-choreoathetosis-liver dysfunction syndrome","type":"Disease"},{"orpha":60,"name":"Alpha-1-antitrypsin deficiency","type":"Disease"},{"orpha":99846,"name":"Autosomal dominant myoglobinuria","type":"Disease"},{"orpha":79345,"name":"Brachytelephalangic chondrodysplasia punctata","type":"Malformation syndrome"},{"orpha":657,"name":"Congenital isolated hyperinsulinism","type":"Clinical group"},{"orpha":99845,"name":"Genetic recurrent myoglobinuria","type":"Disease"},{"orpha":714,"name":"Hemolytic anemia due to diphosphoglycerate mutase deficiency","type":"Disease"},{"orpha":79507,"name":"Hypotonia-failure to thrive-microcephaly syndrome","type":"Disease"},{"orpha":555402,"name":"NAD(P)HX dehydratase deficiency","type":"Disease"},{"orpha":555407,"name":"NAD(P)HX epimerase deficiency","type":"Disease"},{"orpha":289877,"name":"Transient hyperammonemia of the newborn","type":"Particular clinical situation in a disease or syndrome"},{"orpha":727861,"name":"YARS1-related multisystemic disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}