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bn:17270467n
Noun Concept
EN
glycinuria  Glycinuria With or Without Oxalate Nephrolithiasis  Glycinuria With or Without Oxalate Urolithiasis  hyperglycinuria  Iminoglycinuria Type 2
DE
Die Glycinurie ist eine sehr seltene genetisch bedingte Stoffwechselerkrankung des Menschen, bei der es infolge eines Carrierdefektes zu einer erhöhten Ausscheidung der Aminosäure Glycin über den Urin kommt. Wikipedia
Relations
Sources
IS A
hereditary disorder
genetic disease
Amino acid transport disorder
HAS KIND
iminoglycinuria
Adams–Nance syndrome
GENETIC ASSOCIATION
SLC6A19
SLC6A20
Proton-coupled amino acid transporter 2
Wikidata
EN
glycinuria
Wikidata Alias
EN
Glycinuria With or Without Oxalate Nephrolithiasis, Glycinuria With or Without Oxalate Urolithiasis, hyperglycinuria, Iminoglycinuria Type 2

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