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ID

http://id.who.int/icd/entity/753682703

Preferred Name

Déficit en adénosine phosphoribosyltransférase

Definitions

Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive disorder characterized by the formation and hyperexcretion of 2,8-dihydroxyadenine (2,8-DHA) into urine, causing urolithiasis and crystalline nephropathy.

Type

http://www.w3.org/2002/07/owl#Class

comment

la déficience en phosphoribosyltransférase de l'adénine (aprt) est un rare trouble autosomique récessif caractérisé par la formation et l'hyperexcrétion de 2,8-dihydroxyadénine (2,8-dha) dans l'urine, causant urolithiase et néphropathie cristalline.

Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive disorder characterized by the formation and hyperexcretion of 2,8-dihydroxyadenine (2,8-DHA) into urine, causing urolithiasis and crystalline nephropathy.

adenina niedobór fosforu fosforowego (aprt) jest rzadkim zaburzeniem autosomalnej recesywnej charakteryzującej się powstawaniem i hiperexcretion 2,8-dihydroksyadeniny (2,8-dha) do moczu, powodując kamica moczowa i krystaliczna nefropatia.

adenine phosphoribosyltransferase (aprt) deficiency is a rare autosomal recscar disorder χαρακτηρίζεται από το σχηματισμό και υπερέκκριση 2,8-dihydroxyadenine (2,8-dha) στα ούρα, προκαλώντας ουρολιθίαση και κρυσταλλική νεφροπάθεια.

Der Mangel an Adenin-Phosphoribosyltransferase (aprt) ist eine seltene autosomal rezessive Störung, die durch die Bildung und Hyperexkretion von 2,8-Dihydroxyadenin (2,8-dha) in den Urin gekennzeichnet ist und Urolithiasis und kristalline Nephropathie verursacht.

broaderTransitive

http://id.who.int/icd/entity/1958565793

prefLabel

Déficit en adénosine phosphoribosyltransférase

browserUrl

NA

narrowerTransitive

http://id.who.int/icd/entity/1119403628

http://id.who.int/icd/entity/1077306267

label

ανεπάρκειας φωσφόρου φωσφοκρεατίνης ανεπάρκεια

Adenin-Phosphoribosyltransferase-Mangel

adenina niedobór fosfoiodylitransferazy

Adenine phosphoribosyltransferase deficiency

Déficit en adénosine phosphoribosyltransférase

subClassOf

http://id.who.int/icd/entity/1958565793

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