{"orpha":656273,"name":"OBSOLETE: Hypotonia-hypoventilation-intellectual disability-dysautonomia-epilepsy-eye abnormalities syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using HIDEA syndrome","url":"https://raremap.alftech.space/d/ORPHA-656273/","orphanet_url":"https://www.orpha.net/en/disease/detail/656273","names":{"fr":{"name":"OBSOLETE : Syndrome d'hypotonie-hypoventilation-déficience intellectuelle-dysautonomie-épilepsie-anomalies oculaires"},"de":{"name":"OBSOLET: Hypotonie-Hypoventilation-Intelligenzminderung-Dysautonomie-Epilepsie-Augenanomalie-Syndrom","synonyms":["OBSOLET: HIDEA-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome de hipotonía-hipoventilación-discapacidad intelectual-disautonomía-epilepsia-alteraciones oculares","synonyms":["OBSOLETO: Síndrome HIDEA"]},"it":{"name":"OBSOLETO: sindrome ipotonia-ipoventilazione-disabilità intellettiva-disautonomia-epilessia-anomalie oculari","synonyms":["OBSOLETO: Sindrome HIDEA"]},"nl":{"name":"OBSOLEET: Hypotonie - hypoventilatie - intellectuele achterstand - dysautonomie - epilepsie - oogafwijkingen-syndroom","synonyms":["OBSOLEET: HIDEA-syndroom"]},"pt":{"name":"OBSOLETO: Síndrome de hipotonia-hipoventilação-perturbação do desenvolvimento intelectual-disautonomia-epilepsia-anomalias dos olhos","synonyms":["OBSOLETO: Síndrome HIDEA"]},"pl":{"name":"NIEAKTUALNE: Zespół hipotonii-hipowentylacji-niepełnosprawności intelektualnej-dysautonomii-padaczki-nieprawidłowości oczu"},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující hypotonii, hypoventilaci, intelektovou nedostatečnost, dysautonomii, epilepsii a oční abnormality"},"uk":{"name":"ЗАСТАРІЛО: Синдром гіпотонії-гіповентиляції-інтелектуальної недостатності-дисавтономії-епілепсії-аномалій очей"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":436141,"name":"HIDEA syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}