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recessive form of polycystic kidney disease

AttributesValues
rdf:type
owl:sameAs
description
  • مرض يصيب الإنسان (ar)
  • rara malattia che colpisce neonati e bambini e che si caratterizza per la presenza di numerose piccole cisti e dotti dilatati a livello di entrambi i reni e che ha una modalità di trasmissione di tipo autosomico recessivo. (it)
  • recessive form of polycystic kidney disease (en)
  • maladie génétique se manifestant par des dilatations des tubes collecteurs du rein (fr)
  • 多囊性肾脏疾病 (zh)
  • 腎疾患のひとつ (ja)
exact match
exact match
health specialty
DiseasesDB
Disease Ontology ID
NHS Health A to Z ID
health specialty
DiseasesDB
  • 10280
NHS Health A to Z ID
  • autosomal-recessive-polycystic-kidney-disease-arpkd
rdfs:label
  • داء الكلية متعددة الكيسات المتنحي (ar)
  • autosomal recessive polycystic kidney (en)
  • malattia policistica renale autosomica recessiva (it)
  • polykystose rénale type récessif (fr)
  • 常染色体劣性多発性嚢胞腎 (ja)
  • 常染色体隐性多囊肾 (zh)
skos:prefLabel
  • داء الكلية متعددة الكيسات المتنحي (ar)
  • autosomal recessive polycystic kidney (en)
  • malattia policistica renale autosomica recessiva (it)
  • polykystose rénale type récessif (fr)
  • 常染色体劣性多発性嚢胞腎 (ja)
  • 常染色体隐性多囊肾 (zh)
name
  • داء الكلية متعددة الكيسات المتنحي (ar)
  • autosomal recessive polycystic kidney (en)
  • malattia policistica renale autosomica recessiva (it)
  • polykystose rénale type récessif (fr)
  • 常染色体劣性多発性嚢胞腎 (ja)
  • 常染色体隐性多囊肾 (zh)
Freebase ID
Freebase ID
  • /m/04_0m3z
instance of
instance of
subclass of
subclass of
eMedicine ID
eMedicine ID
  • 377154
Orphanet ID
ICD-9-CM
ICD-10-CM
PatientsLikeMe condition ID
GARD rare disease ID
OMIM ID
GeneReviews ID
Orphanet ID
  • 731
ICD-9-CM
  • 753.14
ICD-10-CM
  • Q61.1
PatientsLikeMe condition ID
  • arpkd
GARD rare disease ID
  • 8378
OMIM ID
  • 263200
GeneReviews ID
  • NBK1326
skos:altLabel
  • ARPKD (en)
  • ARPKD (it)
  • ARPKD (ja)
  • Arpkd (en)
  • Autosomal Recessive Polycystic kidney disease (en)
  • Pkhd1 (en)
  • Polycystic Kidney Disease, Infantile, Type I (en)
  • Polycystic Kidney and Hepatic Disease 1 (en)
  • Polycystic kidney, autosomal recessive (en)
  • Polykystose renale type recessif (fr)
  • autosomal recessive polycystic kidney disease (en)
  • obsolete autosomal recessive polycystic kidney (en)
  • Polycystic kidney disease, infantile type (disorder) (en)
  • 常染色体性劣性多発性嚢胞腎 (ja)
OpenAlex ID
NCI Thesaurus ID
UMLS CUI
Quora topic ID
JSTOR topic ID
MeSH descriptor ID
on focus list of Wikimedia project
MedlinePlus ID
MeSH tree code
MeSH descriptor ID
MeSH tree code
OpenAlex ID
  • C2910547607
NCI Thesaurus ID
  • C84579
UMLS CUI
  • C0085548
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