Category:Alport syndrome

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<nowiki>síndrome de Alport; Alport-szindróma; Alport-en sindrome; síndrome d’Alport; Alport-Syndrom; Alport syndrome; نشانگان آلپورت; 奥尔波特综合征; アルポート症候群; Alports syndrom; синдром Альпорта; Альпорт синдромы; Alportin syndrooma; sindromo de Alport; Alportův syndrom; Alportov sindrom; sindrome di Alport; néphropathie par anomalie du collagène IV; Alportov sindrom; ଆଲପୋର୍ଟ ସିଣ୍ଡ୍ରୋମ ‎; Алпортов синдром; Alportov sindrom; תסמונת אלפורט; Ugonjwa wa Alport; syndroom van Alport; กลุ่มอาการอัลพอร์ต; Zespół Alporta; Алпортов синдром; Alport sindromu; Алпортов синдром; síndrome de Alport; 알포트 증후군; Alporti sündroom; Alport syndrome; متلازمة ألبورت; Alportov sindrom; Hội chứng Alport; enfermedad de alport; ensemble de manifestations cliniques qui vont du syndrome d'Alport à une simple hématurie manifestation de la néphropathie à membrane basale fine; ביטוי קליני של מספר פגמים גנטיים; monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss; condizione genetica caratterizzata dalla progressiva perdita di funzione renale e uditiva; Erbkrankheit mit fehlgebildeten Kollagenfasern; ଆଲପୋର୍ଟ ସିଣ୍ଡ୍ରୋମ, ପୂର୍ବ ନାମ ବଂଶାନୁକ୍ରମିକ ନେଫ୍ରାଇଟିସ୍, ଏକ ଜେନେଟିକ ରୋଗ ଯେଉଁଥିରେ ବୃକ୍‌କ ରୋଗ, ଶ୍ରବଣହାନୀ ଏବଂ ଆଖି ସମସ୍ୟା ହୋଇପାରେ |; monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss; مرض وراثي عصبي سمعي; onemocnění; perinnöllinen munuaissairaus; syndroma Alport; Alport症候群; アルポート; Syndrome d'Alport; Syndrôme d'Alport; Nephropathies par anomalie du collagene IV; Néphropathies par anomalie du collagène IV; Альпорта синдром; Malattia di Alport; Nefrite emorragica familiare; hereditary nephritis; nephritis, familial; familial nephritis; Alport's syndrome; سندروم الپورت; نشانگان الپورت; سندروم آلپورت; Progressive hereditäre Nephritis; Alportin oireyhtymä; Alport; hereditary nephritis; nephritis, familial; familial nephritis; Alport's syndrome; متلازمة ألبرت; متلازمة آلبورت; Alport綜合徵; Mal de Alport; Sindrome de Alport; Alport; nefritis hereditaria</nowiki>
Alport syndrome 
monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss
Pèrdua auditiva causada per la síndrome d'Alport en un nen de 13 anys.
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Wikidata Q1331116
Library of Congress authority ID: sh85003837
BabelNet ID: 03596859n
J9U ID: 987007294888205171
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Media in category "Alport syndrome"

The following 2 files are in this category, out of 2 total.