Amino Acid Transport Disorders, Inborn [vrozené poruchy transportu aminokyselin]

topical
1
Terms

aminokyseliny - vrozené poruchy transportu
dědičné poruchy transportu aminokyselin

 

Inborn Transport Disorders, Amino Acid
Inherited Amino Acid Transport Disorders
Transport Disorders, Amino Acid, Inborn

Persistent link   https://www.medvik.cz/link/D020157
Definition

Disorders characterized by defective transport of amino acids across cell membranes. These include deficits in transport across brush-border epithelial cell membranes of the small intestine (MICROVILLI) and KIDNEY TUBULES; transport across the basolateral membrane; and transport across the membranes of intracellular organelles. (From Nippon Rinsho 1992 Jul;50(7):1587-92)

DUI
D020157 MeSH Browser
CUI
M0328095
Previous indexing
Brain Diseases (1966-1976); Brain Diseases, Metabolic (1977-1999)
History note
2000
Public note
2000

C Diseases
C16.320.565.151.355 Hartnup Disease 2
C16.320.565.151.600 Oculocerebrorenal Syndrome 9
C16.320.565.176 Amyloidosis, Familial 16
C16.320.565.595 Lysosomal Storage Diseases 72
C16.320.565.663 Peroxisomal Disorders 20
C16.320.565.753 Progeria 27
C18.452 Metabolic Diseases 1 196
C18.452.648.151.355 Hartnup Disease 2
C18.452.648.151.600 Oculocerebrorenal Syndrome 9
C18.452.648.176 Amyloidosis, Familial 16
C18.452.648.595 Lysosomal Storage Diseases 72
C18.452.648.663 Peroxisomal Disorders 20
C18.452.648.753 Progeria 27