{"orpha":1877,"name":"Muscular dystrophy-white matter spongiosis syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Laminin subunit alpha 2-related congenital muscular dystrophy","url":"https://raremap.alftech.space/d/ORPHA-1877/","orphanet_url":"https://www.orpha.net/en/disease/detail/1877","names":{"fr":{"name":"Syndrome de dystrophie musculaire-substance blanche cérébrale spongieuse"},"de":{"name":"Muskeldystrophie - Spongiosis der weissen Gehirnmasse"},"es":{"name":"Síndrome de distrofia muscular-espongiosis de la sustancia blanca"},"it":{"name":"Sindrome da distrofia muscolare e spongiosi della sostanza bianca"},"nl":{"name":"Spierdystrofie - spongiose van witte stof-syndroom"},"pt":{"name":"Síndrome de distrofia muscular-espongiose da substância branca"},"pl":{"name":"Dystrofia mięśni - zwyrodnienie gąbczaste istoty białej"},"cs":{"name":"Syndrom zahrnující svalovou dystrofii a spongiózu bílé hmoty"},"uk":{"name":"Синдром мязової дистрофії - спонгіозу білої речовини"},"zh":{"name":"肌营养不良-白质海绵状硬化综合征"},"tr":{"name":"Kas distrofisi-beyaz cevher spongioz sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":258,"name":"Laminin subunit alpha 2-related congenital muscular dystrophy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}