Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Iminoglycinuria> ?p ?o }
- Iminoglycinuria abstract "Iminoglycinuria, sometimes called familial iminoglycinuria, is an autosomal recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine, and the imino acids proline and hydroxyproline. This results in excess urinary excretion of all three acids (-uria denotes "in the urine").Iminoglycinuria is a rare and complex disorder, associated with a number of genetic mutations that cause defects in both renal and intestinal transport systems of glycine and imino acids.Imino acids typically contain an imine functional group, instead of the amino group found in amino acids. Proline is considered and usually referred to as an amino acid, but unlike others, it has a secondary amine. This feature, unique to proline, identifies proline also as an imino acid. Hydroxyproline is another imino acid, made from the naturally occurring hydroxylation of proline.".
- Iminoglycinuria icd10 "E72.0".
- Iminoglycinuria icd9 "270.8".
- Iminoglycinuria omim "242600".
- Iminoglycinuria thumbnail Imine.png?width=300.
- Iminoglycinuria wikiPageID "20900477".
- Iminoglycinuria wikiPageLength "21798".
- Iminoglycinuria wikiPageOutDegree "99".
- Iminoglycinuria wikiPageRevisionID "645001499".
- Iminoglycinuria wikiPageWikiLink Active_transport.
- Iminoglycinuria wikiPageWikiLink Adenosine_triphosphate.
- Iminoglycinuria wikiPageWikiLink Alanine.
- Iminoglycinuria wikiPageWikiLink Allele.
- Iminoglycinuria wikiPageWikiLink Amine.
- Iminoglycinuria wikiPageWikiLink Amino_acid.
- Iminoglycinuria wikiPageWikiLink Autosome.
- Iminoglycinuria wikiPageWikiLink Blindness.
- Iminoglycinuria wikiPageWikiLink Brain.
- Iminoglycinuria wikiPageWikiLink Brush_border.
- Iminoglycinuria wikiPageWikiLink Catabolism.
- Iminoglycinuria wikiPageWikiLink Category:Amino_acid_metabolism_disorders.
- Iminoglycinuria wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Iminoglycinuria wikiPageWikiLink Category:Nephrology.
- Iminoglycinuria wikiPageWikiLink Category:Rare_diseases.
- Iminoglycinuria wikiPageWikiLink Cecum.
- Iminoglycinuria wikiPageWikiLink Cell_membrane.
- Iminoglycinuria wikiPageWikiLink Central_nervous_system.
- Iminoglycinuria wikiPageWikiLink Chloride.
- Iminoglycinuria wikiPageWikiLink Choroid.
- Iminoglycinuria wikiPageWikiLink Co-transport.
- Iminoglycinuria wikiPageWikiLink Colon_(anatomy).
- Iminoglycinuria wikiPageWikiLink Concentration_gradient.
- Iminoglycinuria wikiPageWikiLink Cotransporter.
- Iminoglycinuria wikiPageWikiLink Cysteine.
- Iminoglycinuria wikiPageWikiLink Deafness.
- Iminoglycinuria wikiPageWikiLink Digestion.
- Iminoglycinuria wikiPageWikiLink Dominance_(genetics).
- Iminoglycinuria wikiPageWikiLink Duodenum.
- Iminoglycinuria wikiPageWikiLink Encephalopathy.
- Iminoglycinuria wikiPageWikiLink Epithelium.
- Iminoglycinuria wikiPageWikiLink Excretion.
- Iminoglycinuria wikiPageWikiLink Facilitated_diffusion.
- Iminoglycinuria wikiPageWikiLink File:Autorecessive.svg.
- Iminoglycinuria wikiPageWikiLink Functional_group.
- Iminoglycinuria wikiPageWikiLink Gastrointestinal_tract.
- Iminoglycinuria wikiPageWikiLink Gene.
- Iminoglycinuria wikiPageWikiLink Genetic_carrier.
- Iminoglycinuria wikiPageWikiLink Glomerulus.
- Iminoglycinuria wikiPageWikiLink Glycine.
- Iminoglycinuria wikiPageWikiLink Gyrate_atrophy.
- Iminoglycinuria wikiPageWikiLink Hartnup_disease.
- Iminoglycinuria wikiPageWikiLink Hearing_loss.
- Iminoglycinuria wikiPageWikiLink Heterozygous.
- Iminoglycinuria wikiPageWikiLink Homozygous.
- Iminoglycinuria wikiPageWikiLink Human.
- Iminoglycinuria wikiPageWikiLink Hydroxylation.
- Iminoglycinuria wikiPageWikiLink Hydroxyproline.
- Iminoglycinuria wikiPageWikiLink Hypertension.
- Iminoglycinuria wikiPageWikiLink Ileum.
- Iminoglycinuria wikiPageWikiLink Imine.
- Iminoglycinuria wikiPageWikiLink Imino_acid.
- Iminoglycinuria wikiPageWikiLink Inborn_errors_of_renal_tubular_transport.
- Iminoglycinuria wikiPageWikiLink Integral_membrane_protein.
- Iminoglycinuria wikiPageWikiLink Intellectual_disability.
- Iminoglycinuria wikiPageWikiLink Ion_channel.
- Iminoglycinuria wikiPageWikiLink Jejunum.
- Iminoglycinuria wikiPageWikiLink Kidney.
- Iminoglycinuria wikiPageWikiLink Kidney_stone.
- Iminoglycinuria wikiPageWikiLink Large_intestine.
- Iminoglycinuria wikiPageWikiLink Lumen_(anatomy).
- Iminoglycinuria wikiPageWikiLink Mammal.
- Iminoglycinuria wikiPageWikiLink Membrane_transport_protein.
- Iminoglycinuria wikiPageWikiLink Membrane_transport_proteins.
- Iminoglycinuria wikiPageWikiLink Mental_retardation.
- Iminoglycinuria wikiPageWikiLink Messenger_RNA.
- Iminoglycinuria wikiPageWikiLink Microglia.
- Iminoglycinuria wikiPageWikiLink Molecular_diffusion.
- Iminoglycinuria wikiPageWikiLink Mutation.
- Iminoglycinuria wikiPageWikiLink K+-ATPase.
- Iminoglycinuria wikiPageWikiLink Na-K-Cl_cotransporter.
- Iminoglycinuria wikiPageWikiLink Nephron.
- Iminoglycinuria wikiPageWikiLink Oral_rehydration_therapy.
- Iminoglycinuria wikiPageWikiLink Organ_(anatomy).
- Iminoglycinuria wikiPageWikiLink Organ_(biology).
- Iminoglycinuria wikiPageWikiLink Ornithine.
- Iminoglycinuria wikiPageWikiLink Ornithine_translocase_deficiency.
- Iminoglycinuria wikiPageWikiLink Penetrance.
- Iminoglycinuria wikiPageWikiLink Phenotype.
- Iminoglycinuria wikiPageWikiLink Pipecolate.
- Iminoglycinuria wikiPageWikiLink Pipecolic_acid.
- Iminoglycinuria wikiPageWikiLink Proline.
- Iminoglycinuria wikiPageWikiLink Proximal_convoluted_tubule.
- Iminoglycinuria wikiPageWikiLink Proximal_tubule.
- Iminoglycinuria wikiPageWikiLink Reabsorption.
- Iminoglycinuria wikiPageWikiLink Retina.
- Iminoglycinuria wikiPageWikiLink SLC36A1.
- Iminoglycinuria wikiPageWikiLink SLC36A2.
- Iminoglycinuria wikiPageWikiLink SLC6A18.
- Iminoglycinuria wikiPageWikiLink SLC6A19.
- Iminoglycinuria wikiPageWikiLink SLC6A20.