{"orpha":156643,"name":"Genetic endocrine growth 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-156643/","orphanet_url":"https://www.orpha.net/en/disease/detail/156643","names":{"fr":{"name":"Maladie endocrinienne génétique de la croissance"},"de":{"name":"Wachstumsstörung, endokrine, genetisch bedingte"},"es":{"name":"Enfermedad endocrina genética del crecimiento"},"it":{"name":"Malattia endocrina della crescita, tipo genetico"},"nl":{"name":"Genetische endocriene groeiziekte"},"pt":{"name":"Doença endócrina do crescimento, genética"},"pl":{"name":"Genetyczna endokrynologiczna choroba wzrostu"},"cs":{"name":"Geneticky podmíněná endokrinní porucha růstu"},"uk":{"name":"Генетично обумовлене ендокринне захворювання росту"},"zh":{"name":"遗传性内分泌生生长疾病"},"tr":{"name":"Genetik endokrin büyüme hastalığı"}},"xrefs":[{"source":"MONDO","code":"15514","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680637","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":156638,"name":"Rare genetic endocrine disease","classifications":[156]}],"children":[{"orpha":436174,"name":"Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome","type":"Disease"},{"orpha":418,"name":"Congenital adrenal hyperplasia","type":"Clinical group"},{"orpha":54595,"name":"Craniopharyngioma","type":"Disease"},{"orpha":435554,"name":"Genetic precocious puberty","type":"Category"},{"orpha":181393,"name":"Growth hormone insensitivity syndrome","type":"Category"},{"orpha":85173,"name":"IMAGe syndrome","type":"Malformation syndrome"},{"orpha":494433,"name":"MIRAGE syndrome","type":"Disease"},{"orpha":95488,"name":"Non-acquired pituitary hormone deficiency","type":"Category"},{"orpha":226292,"name":"Permanent congenital hypothyroidism","type":"Category"},{"orpha":95709,"name":"Rare acquired premature ovarian failure","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}