Infobox_Disease
Name = PAGENAME
Caption =
DiseasesDB =
ICD10 = ICD10|E|72|0|e|70
ICD9 = ICD9|270
ICDO =
OMIM =
MedlinePlus =
eMedicineSubj =
eMedicineTopic =
MeshID = D020157
Amino acid transport disorders are medical conditions associated with a failure of
An example is
External links
* http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1176258
Wikimedia Foundation. 2010.
amino acid — Biochem. any of a class of organic compounds that contains at least one amino group, NH2, and one carboxyl group, COOH: the alpha amino acids, RCH(NH2)COOH, are the building blocks from which proteins are constructed. Cf. essential amino acid.… … Universalium
Transport disease, cystine — Commonly known as cystinuria, this is an inherited (genetic) disorder of the transport of an amino acid (a building block of protein) called cystine. The result is an excess of cystine in the urine (cystinuria) and the formation of cystine stones … Medical dictionary
Acid alpha-glucosidase — Glucosidase, alpha; acid, also known as GAA, is a human gene.cite web | title = Entrez Gene: GAA glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView … Wikipedia
Glutamic acid — Glutamic acid … Wikipedia
Cystine transport disease — Commonly known as cystinuria, this is an inherited (genetic) disorder of the transport of an amino acid (a building block of protein) called cystine resulting in an excess of cystine in the urine (cystinuria) and the formation of cystine stones.… … Medical dictionary
Disease, cystine transport — Commonly known as cystinuria, this is an inherited (genetic) disorder of the transport of an amino acid (a building block of protein) called cystine resulting in an excess of cystine in the urine (cystinuria) and the formation of cystine stones.… … Medical dictionary
Clavulanic acid — Systematic (IUPAC) name … Wikipedia
congenital disorder — Structural abnormality (e.g., atresia, agenesis), functional problem (e.g., cystic fibrosis, phenylketonuria), or disease present at birth. Almost all are due to genetic factors (inherited or spontaneous mutations, chromosomal disorders),… … Universalium
Gamma-Hydroxybutyric acid — γ Hydroxybutyric acid Systematic (IUPAC) name 4 Hydroxybutanoic acid … Wikipedia
Iminoglycinuria — Classification and external resources Imine, a functional group found in imino acids ICD 10 E72.0 … Wikipedia
