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bn:17270467n
Noun Concept
IT
No term available
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
malattia ereditaria
malattia genetica
EN
Amino acid transport disorder
HAS KIND
EN
iminoglycinuria
EN
Adams–Nance syndrome
GENETIC ASSOCIATION
SLC6A19
SLC6A20
EN
Proton-coupled amino acid transporter 2

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