About: Autosomal dominant polycystic kidney disease

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Autosomal recessive polycystic kidney disease (ARPKD) is the recessive form of polycystic kidney disease. It is associated with a group of congenital fibrocystic syndromes. Mutations in the PKHD1 (chromosomal locus 6p12.2) cause ARPKD.

Attributes	Values
rdf:type	Thing Fuchs' dystrophy yago:Abstraction100002137 yago:Attribute100024264 yago:Condition113920835 yago:Disease114070360 yago:GeneticDisease114151139 yago:IllHealth114052046 yago:Illness114061805 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:WikicatGeneticDisorders disease yago:State100024720 umbel-rc:AilmentCondition
rdfs:label	Autosomal recessive polycystic kidney disease (en) داء الكلية متعددة الكيسات المتنحي (ar) Polykystose rénale autosomique récessive (fr) Malattia policistica renale autosomica recessiva (it) 常染色体劣性多発性嚢胞腎 (ja)
rdfs:comment	داء الكلية متعددة الكيسات المتنحي هو أحد نوعي داء الكلية متعددة الكيسات وأقلها حدوثًا (أقل من 10% من الحالات) ولكنه الأكثر خطورة، ويحدث تكيس الكلية عادة لدى الأطفال. الوالدين قد يكونون سليمين ولكن يحملون المرض. الجين المؤثر chromosomal locus 6p12.2 (ar) Autosomal recessive polycystic kidney disease (ARPKD) is the recessive form of polycystic kidney disease. It is associated with a group of congenital fibrocystic syndromes. Mutations in the PKHD1 (chromosomal locus 6p12.2) cause ARPKD. (en) La polykystose rénale autosomique récessive ou Rein polykystique autosomique récessif est une maladie génétique se manifestant par des dilatations des tubes collecteurs du rein et des canaux hépatiques collectant la bile, responsable d’une insuffisance rénale et insuffisance hépatique. Les manifestations de cette maladie apparaissent souvent dans la vie fœtale. La période néonatale est une période à mortalité importante (20 %) par hypoplasie pulmonaire. (fr) 常染色体劣性多発性嚢胞腎（じょうせんしょくたいれっせいたはつせいのうほうじん、英: autosomal recessive polycystic kidney disease, ARPKD）は、腎疾患のひとつ。多発性嚢胞腎の1タイプであり、新生児にみられ羊水過少による肺低形成などを伴いポッター症候群のⅠ型に分類される。 (ja) La malattia policistica renale autosomica recessiva o semplicemente malattia policistica renale infantile è una 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)
foaf:name	Autosomal recessive polycystic kidney disease (en)
name	Autosomal recessive polycystic kidney disease (en)
foaf:depiction
dcterms:subject	Kidney diseases Rare diseases Ciliopathy
Wikipage page ID	20332785 (xsd:integer)
Wikipage revision ID	1109053367 (xsd:integer)
Link from a Wikipage to another Wikipage	Pre-eclampsia Nonsense mutation End-stage kidney disease Kidney diseases Antibiotic Compound heterozygosity Polydipsia Autosomal dominant polycystic kidney disease Cell division Acute kidney injury Potter sequence Rare diseases Abdominal mass Ciliopathy Kidney dialysis Kidney transplantation Symptoms Autosomal dominant polycystic kidney disease Fibrocystin Recessive gene Centrosomes Medical sign Oligohydramnios Polyuria PKHD1 Mitotic spindle Abdominal discomfort Ultrasonography
sameAs	Autosomal dominant polycystic kidney disease Autosomal dominant polycystic kidney disease Autosomal dominant polycystic kidney disease Autosomal dominant polycystic kidney disease Autosomal dominant polycystic kidney disease Autosomal dominant polycystic kidney disease Autosomal dominant polycystic kidney disease Autosomal dominant polycystic kidney disease
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:Cite_journal dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Scholia dbt:Congenital_malformations_of_urinary_system dbt:Ciliopathy dbt:Cystic_diseases
thumbnail	wiki-commons:Special:FilePath/autorecessive.svg?width=300
diagnosis	Ultrasound (en)
DiseasesDB	10280 (xsd:integer)
ICD	753.100000 (xsd:double) (en) Q61. (en)
MeshID	D017044 (en)
OMIM	263200 (xsd:integer)
Orphanet	731 (xsd:integer)
symptoms	Polyuria (en)
treatment	Medications for hypertension (en)
caption	ARPKD is inherited in an autosomal recessive pattern (en)
causes	Mutations in the PKHD1 gene (en)
MedlinePlus	502 (xsd:integer)
synonyms	ARPKD (en)
has abstract	داء الكلية متعددة الكيسات المتنحي هو أحد نوعي داء الكلية متعددة الكيسات وأقلها حدوثًا (أقل من 10% من الحالات) ولكنه الأكثر خطورة، ويحدث تكيس الكلية عادة لدى الأطفال. الوالدين قد يكونون سليمين ولكن يحملون المرض. الجين المؤثر chromosomal locus 6p12.2 (ar) Autosomal recessive polycystic kidney disease (ARPKD) is the recessive form of polycystic kidney disease. It is associated with a group of congenital fibrocystic syndromes. Mutations in the PKHD1 (chromosomal locus 6p12.2) cause ARPKD. (en) La polykystose rénale autosomique récessive ou Rein polykystique autosomique récessif est une maladie génétique se manifestant par des dilatations des tubes collecteurs du rein et des canaux hépatiques collectant la bile, responsable d’une insuffisance rénale et insuffisance hépatique. Les manifestations de cette maladie apparaissent souvent dans la vie fœtale. La période néonatale est une période à mortalité importante (20 %) par hypoplasie pulmonaire. (fr)

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