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Amino Acid Transport Disorders, Inborn MeSH Descriptor Data 2023


MeSH Heading
Amino Acid Transport Disorders, Inborn
Tree Number(s)
C16.320.565.151
C18.452.648.151
Unique ID
D020157
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D020157
Scope Note
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)
Entry Version
AA TRANSPORT DIS INBORN
Entry Term(s)
Inborn Transport Disorders, Amino Acid
Inherited Amino Acid Transport Disorders
Transport Disorders, Amino Acid, Inborn
Previous Indexing
Brain Diseases (1966-1976)
Brain Diseases, Metabolic (1977-1999)
Public MeSH Note
2000
History Note
2000
Date Established
2000/01/01
Date of Entry
1999/11/08
Revision Date
2006/07/05
Amino Acid Transport Disorders, Inborn Preferred
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