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Autosomal recessive disease characterized by the buildup of mucus

Property Value
dbo:description
  • Krankheit (de)
  • lidská nemoc (cs)
  • malattia dell'apparato respiratorio (it)
  • autosomal recessive disease characterized by the buildup of mucus (en)
  • recessief genetische ziekte die progressieve invaliditeit veroorzakende invloed heeft op het gehele lichaam dikwijls leidend tot voortijdig overlijden (nl)
  • Pankreako eta biriketako sortzetiko malformazioa. Sabel handia, eginkai ugariak, bronkiektasiak eta gantzekiko jasanezintasuna dira bere sintomak (eu)
  • مرض وراثي صبغي جسمي متنحّ يحدث بسببه عجز مترقٍّ في عمل الغدد خارجية الإفراز، مما يُؤثر على وظائف متعددة في الجسم (ar)
  • afiechyd sy'n ymwneud mwcws (cy)
  • aineenvaihduntasairaus (fi)
  • 점액의 축적을 특징으로 하는 상염색체 열성 질환 (ko)
  • enfermidade das glándulas exócrinas (gl)
  • genetika malsano (eo)
  • genetikai betegség (hu)
  • maladie génétique (fr)
  • malaltia hereditària (ca)
  • recessiv genetisk sjukdom (sv)
  • enfermedad autosómica recesiva que afecta principalmente a los pulmones (es)
  • outosomaal resessiewe siekte wat gekenmerk word deur die opbou van slym (af)
  • avtosomno recesivna bolezen, za katero je značilno kopičenje sluzi (sl)
  • автоімунна спадкова хвороба (uk)
  • 临床表现为慢性咳嗽和喘鸣,与反复或慢性肺部感染有关的一种常染色体隐性遗传性疾病 (zh)
  • doença genética que afeta principalmente os pulmões (pt)
  • Çoğunlukla akciğerleri etkileyen otozomal resesif hastalık (tr)
  • наследственное заболевание, характеризующееся поражением желëз внешней секреции, нарушенией функций органов дыхания (ru)
  • מחלה תורשתית (iw)
  • بیماری متابولیک ارثی (fa)
dbo:diseasesDB
  • 3347
dbo:eMedicineSubject
  • article (en)
dbo:eMedicineTopic
  • 1001602 (en)
dbo:geneReviewsName
  • CFTR-Related Disorders (en)
dbo:icd10
  • E84.
dbo:icd9
  • 277.0
dbo:medicalCause
dbo:medicalDiagnosis
dbo:medlinePlus
  • 000107
dbo:meshId
  • D003550
dbo:omim
  • 219700 (xsd:integer)
dbo:orpha
  • 586
dbo:symptom
dbo:thumbnail
dbo:treatment
dbo:wikiPageExternalLink
dbo:wikiPageWikiLink
dbp:causes
  • Genetic (en)
dbp:deaths
  • 40 (xsd:integer)
dbp:diagnosis
dbp:diseasesdb
  • 3347 (xsd:integer)
dbp:displayAuthors
  • 6 (xsd:integer)
dbp:duration
  • Long term (en)
dbp:emedicinesubj
  • article (en)
dbp:emedicinetopic
  • 1001602 (xsd:integer)
dbp:field
dbp:frequency
  • 1 (xsd:integer)
  • (en)
dbp:genereviewsid
  • NBK1250 (en)
dbp:genereviewsname
  • CFTR-Related Disorders (en)
dbp:icd
  • 277 (xsd:integer)
  • (en)
  • E84. (en)
dbp:medlineplus
  • 107 (xsd:integer)
dbp:meshid
  • D003550 (en)
dbp:name
  • Cystic fibrosis (en)
dbp:nameListStyle
  • vanc (en)
dbp:omim
  • 219700 (xsd:integer)
dbp:onset
  • 1.57788E7 (dbd:second)
dbp:orphanet
  • 586 (xsd:integer)
dbp:prognosis
  • 1.57788E9 (dbd:second)
dbp:risks
  • Genetic (en)
dbp:symptoms
  • Difficulty breathing, coughing up mucus, poor growth, fatty stool (en)
dbp:synonyms
  • Mucoviscidosis (en)
dbp:treatment
  • Physiotherapy, antibiotics, pancreatic enzyme replacement, cystic fibrosis transmembrane conductance regulator modulators, lung transplantation (en)
dbp:wikiPageUsesTemplate
dbp:wordnet_type
dct:subject
gold:hypernym
rdf:type
rdfs:label
  • Cystic fibrosis (en)
  • تليف كيسي (ar)
  • Fibrosi quística (ca)
  • Cystická fibróza (cs)
  • Mukoviszidose (de)
  • Κυστική ίνωση (el)
  • Mukoviskozeco (eo)
  • Fibrosis quística (es)
  • Fibrosi kistiko (eu)
  • Fiobróis chisteach (ga)
  • Mucoviscidose (fr)
  • Fibrosis sistik (in)
  • Fibrosi cistica (it)
  • 嚢胞性線維症 (ja)
  • Taaislijmziekte (nl)
  • 낭포성 섬유증 (ko)
  • Fibrose cística (pt)
  • Муковисцидоз (ru)
  • Mukowiscydoza (pl)
  • Cystisk fibros (sv)
  • 囊腫性纖維化 (zh)
  • Муковісцидоз (uk)
rdfs:seeAlso
owl:sameAs
skos:closeMatch
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • Cystic fibrosis (en)
is dbo:academicDiscipline of
is dbo:deathCause of
is dbo:differentialDiagnosis of
is dbo:knownFor of
is dbo:medicalCause of
is dbo:wikiPageDisambiguates of
is dbo:wikiPageRedirects of
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is dbp:deathCause of
is dbp:differential of
is dbp:fields of
is dbp:focus of
is dbp:knownFor of
is dbp:risks of
is foaf:primaryTopic of
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