{"orpha":3084,"name":"Mirhosseini-Holmes-Walton syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Pigmentary retinopathy-intellectual disability syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cohen syndrome","url":"https://raremap.alftech.space/d/ORPHA-3084/","orphanet_url":"https://www.orpha.net/en/disease/detail/3084","names":{"fr":{"name":"Syndrome de Mirhosseini-Holmes-Walton","synonyms":["Syndrome de rétinite pigmentaire-déficience intellectuelle"]},"de":{"name":"Mirhosseini-Holmes-Walton-Syndrom","synonyms":["Pigmentretinopathie-Intelligenzminderung-Syndrom"]},"es":{"name":"Síndrome de Morhosseini-Holmes-Walton","synonyms":["Síndrome de retinopatía pigmentaria-discapacidad intelectual"]},"it":{"name":"Sindrome di Morhosseini-Holmes-Walton","synonyms":["Sindrome retinite pigmentosa-disabilità intellettiva"]},"nl":{"name":"Syndroom van Mirhosseini-Holmes-Walton","synonyms":["Pigmentretinopathie - intellectuele achterstand-syndroom"]},"pt":{"name":"Síndrome Morhosseini-Holmes-Walton","synonyms":["Síndrome de retinopatia pigmentosa-perturbação do desenvolvimento intelectual"]},"pl":{"name":"Zespół Mirhosseini, Holmesa i Waltona","synonyms":["Retinopatia barwnikowa - niepełnosprawność intelektualna"]},"cs":{"name":"Mirhosseiniho-Holmesův-Waltonův syndrom","synonyms":["Syndrom zahrnující pigmentovou retinopatii a mentální retardaci","Mirhosseini-Holmes-Waltonův syndrom"]},"uk":{"name":"Синдром Мірхосейні-Холмса-Уолтона","synonyms":["Синдром пігментної ретинопатії - інтелектуальної недостатності"]},"zh":{"name":"Mirhosseini-Holmes-Walton综合征","synonyms":["色素性视网膜病-智力障碍综合征"]},"tr":{"name":"Mirhosseini-Holmes-Walton sendromu","synonyms":["Pigmenter retinopati-zihinsel yetersizlik sendromu"]}},"xrefs":[{"source":"OMIM","code":"268050","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0796072","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":193,"name":"Cohen syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}