{"orpha":2675,"name":"OBSOLETE: Neuroaxonal dystrophy-renal tubular acidosis syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Maccario-Mena syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Primary renal tubular acidosis","url":"https://raremap.alftech.space/d/ORPHA-2675/","orphanet_url":"https://www.orpha.net/en/disease/detail/2675","names":{"fr":{"name":"OBSOLETE : Syndrome de dystrophie neuroaxonale-acidose tubulaire","synonyms":["OBSOLETE : Syndrome de Maccario-Mena"]},"de":{"name":"OBSOLET: Neuroaxonale Dystrophie-renale tubuläre Azidose-Syndrom","synonyms":["OBSOLET: Maccario-Mena-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome de distrofia neuroaxonal-acidosis tubular renal","synonyms":["OBSOLETO: Síndrome de Maccario-Mena"]},"it":{"name":"OBSOLETO: Sindrome distrofia neuroassonale-acidosi tubulare renale","synonyms":["OBSOLETO: Sindrome di Maccario-Mena"]},"nl":{"name":"OBSOLEET: Neuroaxonale dystrofie - renale tubulaire acidose-syndroom","synonyms":["OBSOLEET: Syndroom van Maccario-Mena"]},"pt":{"name":"OBSOLETO: Síndrome de distrofia neuroaxonal-acidose tubular renal","synonyms":["OBSOLETO: Síndrome Maccario-Mena"]},"pl":{"name":"NIEAKTUALNE: Dystrofia neuroaksonalna - kwasica nerkowo-kanalikowa","synonyms":["NIEAKTUALNE: Zespół Maccario i Mena"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující neuroaxiální dystrofii a renální tubulární acidózu","synonyms":["OBSOLETE: Maccario-Mena syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Синдром нейроаксональної дистрофії - ниркового тубулярного ацидозу","synonyms":["ЗАСТАРІЛО: Синдром Маккаріо-Мена"]},"zh":{"name":"弃用：神经轴性营养不良-肾小管性酸中毒","synonyms":["Maccario-Mena综合征"]},"tr":{"name":"Eski adı: Nöroaksonal distrofi-renal tübüler asidoz sendromu","synonyms":["Maccario-Mena sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":314822,"name":"Primary renal tubular acidosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}