About: Alport syndrome

Property	Value
dbo:description	onemocnění (cs) ensemble de manifestations cliniques qui vont du syndrome d'Alport à une simple hématurie manifestation de la néphropathie à membrane basale fine (fr) ביטוי קליני של מספר פגמים גנטיים (iw) Erbkrankheit mit fehlgebildeten Kollagenfasern (de) condizione genetica caratterizzata dalla progressiva perdita di funzione renale e uditiva (it) monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss (en) enfermedad de alport (es) perinnöllinen munuaissairaus (fi) ଆଲପୋର୍ଟ ସିଣ୍ଡ୍ରୋମ, ପୂର୍ବ ନାମ ବଂଶାନୁକ୍ରମିକ ନେଫ୍ରାଇଟିସ୍, ଏକ ଜେନେଟିକ ରୋଗ ଯେଉଁଥିରେ ବୃକ୍‌କ ରୋଗ, ଶ୍ରବଣହାନୀ ଏବଂ ଆଖି ସମସ୍ୟା ହୋଇପାରେ \| (or) مرض وراثي عصبي سمعي (ar)
dbo:diseasesDB	454
dbo:eMedicineSubject	med (en)
dbo:eMedicineTopic	110 (en)
dbo:geneReviewsId	NBK1207
dbo:geneReviewsName	Collagen IV-Related Nephropathies (Alport Syndrome and Thin Basement Membrane Nephropathy) (en)
dbo:icd10	Q87.8
dbo:icd9	759.89
dbo:medlinePlus	000504
dbo:meshId	D009394 y
dbo:omim	301050 (xsd:integer)
dbo:orpha	63
dbo:thumbnail	wiki-commons:Special:FilePath/Alport_haring_loss.jpg?width=300
dbo:wikiPageExternalLink	https://ghr.nlm.nih.gov/condition/alport-syndrome https://www.ncbi.nlm.nih.gov/books/NBK1207/
dbo:wikiPageWikiLink	dbr:Samoyed_hereditary_glomerulopathy dbr:X_chromosome dbr:Goodpasture_syndrome dbr:Thin_basement_membrane_disease dbc:Syndromes_affecting_the_kidneys dbr:Aortic_dissection dbr:Kidney_transplantation dbr:Macula dbr:Basement_membrane dbr:Cataract dbc:Collagen_disease dbr:Type_IV_collagen dbr:Gene_therapy dbr:Hematuria dbr:Human_eye dbr:Keratoconus dbr:Kidney_dialysis dbc:Kidney_diseases dbr:Fechtner_syndrome dbr:Recurrent_corneal_erosion dbr:Proteinuria dbr:Ear dbr:Genetic_disorder dbr:Kidney dbr:Leiomyoma dbr:AMMECR1 dbr:Lenticonus dbr:Chronic_kidney_disease dbr:Mutation dbr:Podocyte dbr:Glomerulonephritis dbr:Retinitis_pigmentosa dbr:Urine_test_strip dbc:Syndromes_with_tumors dbc:Syndromes_affecting_hearing dbr:Autosomal_dominant dbr:ACE_inhibitor dbr:Corneal_transplant dbr:X-linked dbr:MYH9 dbr:Contact_lenses dbr:Autosomal_recessive dbr:Chromosome_2_(human) dbr:Cecil_A._Alport dbr:COL4A3 dbr:COL4A4 dbr:COL4A5
dbp:article	Alport syndrome (en)
dbp:caption	Hearing loss effect of Alport syndrome in 13-year-old boy (en)
dbp:diseasesdb	454 (xsd:integer)
dbp:emedicinesubj	med (en)
dbp:emedicinetopic	110 (xsd:integer)
dbp:genereviewsname	Collagen IV-Related Nephropathies (en)
dbp:genereviewsnbk	NBK1207 (en)
dbp:icd	759.890000 (xsd:double) (en) Q87.8 (en)
dbp:medlineplus	504 (xsd:integer)
dbp:meshid	2.964520944E11 (dbd:second)
dbp:name	Alport syndrome (en)
dbp:omim	301050 (xsd:integer)
dbp:orphanet	63 (xsd:integer)
dbp:url	https://ghr.nlm.nih.gov/condition/alport-syndrome
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dbp:wordnet_type	http://www.w3.org/2006/03/wn/wn20/instances/synset-disease-noun-1
dct:subject	dbc:Syndromes_affecting_the_kidneys dbc:Collagen_disease dbc:Kidney_diseases dbc:Diseases_named_after_discoverers dbc:Rare_syndromes dbc:Syndromes_with_tumors dbc:Syndromes_affecting_hearing
gold:hypernym	dbr:Disorder
rdf:type	owl:Thing wikidata:Q12136
rdfs:label	Alport syndrome (en) متلازمة ألبورت (ar) Síndrome d'Alport (ca) Alport-Syndrom (de) Alportův syndrom (cs) Síndrome de Alport (es) Néphropathies par anomalie du collagène IV (fr) Sindrome di Alport (it) アルポート症候群 (ja) Syndroom van Alport (nl) Zespół Alporta (pl) 알포트 증후군 (ko) Síndrome de Alport (pt) Синдром Альпорта (uk) Alports syndrom (sv)
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skos:closeMatch	http://www.springernature.com/scigraph/things/subjects/alport-syndrome
prov:wasDerivedFrom	wikipedia-en:Alport_syndrome?oldid=1293500784&ns=0
foaf:depiction	wiki-commons:Special:FilePath/Alport_haring_loss.jpg
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foaf:name	Alport syndrome (en)
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