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- Ornithine_aminotransferase_deficiency abstract "Ornithine aminotransferase deficiency (also known as gyrate atrophy of the choroid and retina) is an inborn error of ornithine metabolism, caused by decreased activity of the enzyme ornithine aminotransferase. Biochemically, it can be detected by elevated levels of ornithine in the blood. Clinically, it presents initially with poor night vision, which slowly progresses to total blindness. It is believed to be inherited in an autosomal recessive manner. Approximately 200 known cases have been reported in the literature. The incidence is highest in Finland, estimated at 1:50,000.".
- Ornithine_aminotransferase_deficiency omim "258870".
- Ornithine_aminotransferase_deficiency thumbnail L-Ornithine_structure.svg?width=300.
- Ornithine_aminotransferase_deficiency wikiPageID "36812289".
- Ornithine_aminotransferase_deficiency wikiPageLength "4730".
- Ornithine_aminotransferase_deficiency wikiPageOutDegree "38".
- Ornithine_aminotransferase_deficiency wikiPageRevisionID "692921500".
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Allele.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Amino_acid.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Blood_plasma.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Cataract.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Category:Amino_acid_metabolism_disorders.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Category:Inborn_errors_of_metabolism.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Chromosome_10_(human).
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Dark_adaptation_threshold.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Dominance_(genetics).
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Electroretinography.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Enzyme.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Fibroblast.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Finland.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Gene.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Homocitrulline.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Hyperammonemia.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Lymphoblast.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Mutation.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Myopia.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Newborn_screening.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Night_vision.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Nyctalopia.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Ophthalmology.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Ornithine.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Ornithine_aminotransferase.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Ornithine_transcarbamylase_deficiency.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Ornithine_translocase_deficiency.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Orotic_acid.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Urea_cycle.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Urea_cycle_disorder.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Urine.
- Ornithine_aminotransferase_deficiency wikiPageWikiLink Visual_impairment.
- Ornithine_aminotransferase_deficiency wikiPageWikiLinkText "Gyrate atrophy of the retina and choroid".
- Ornithine_aminotransferase_deficiency wikiPageWikiLinkText "Ornithine aminotransferase deficiency".
- Ornithine_aminotransferase_deficiency wikiPageWikiLinkText "ornithine aminotransferase deficiency".
- Ornithine_aminotransferase_deficiency caption Ornithine.
- Ornithine_aminotransferase_deficiency name "Ornithine aminotransferase deficiency".
- Ornithine_aminotransferase_deficiency omim "258870".
- Ornithine_aminotransferase_deficiency wikiPageUsesTemplate Template:Infobox_disease.
- Ornithine_aminotransferase_deficiency wikiPageUsesTemplate Template:Reflist.
- Ornithine_aminotransferase_deficiency subject Category:Amino_acid_metabolism_disorders.
- Ornithine_aminotransferase_deficiency subject Category:Autosomal_recessive_disorders.
- Ornithine_aminotransferase_deficiency subject Category:Inborn_errors_of_metabolism.
- Ornithine_aminotransferase_deficiency hypernym Error.
- Ornithine_aminotransferase_deficiency type Disease.
- Ornithine_aminotransferase_deficiency type Defect.
- Ornithine_aminotransferase_deficiency type Disorder.
- Ornithine_aminotransferase_deficiency type Error.
- Ornithine_aminotransferase_deficiency type Pediatric.
- Ornithine_aminotransferase_deficiency type Thing.
- Ornithine_aminotransferase_deficiency type Q12136.
- Ornithine_aminotransferase_deficiency comment "Ornithine aminotransferase deficiency (also known as gyrate atrophy of the choroid and retina) is an inborn error of ornithine metabolism, caused by decreased activity of the enzyme ornithine aminotransferase. Biochemically, it can be detected by elevated levels of ornithine in the blood. Clinically, it presents initially with poor night vision, which slowly progresses to total blindness. It is believed to be inherited in an autosomal recessive manner.".
- Ornithine_aminotransferase_deficiency label "Ornithine aminotransferase deficiency".
- Ornithine_aminotransferase_deficiency sameAs Q7103623.
- Ornithine_aminotransferase_deficiency sameAs m.0ll45s_.
- Ornithine_aminotransferase_deficiency sameAs Q7103623.
- Ornithine_aminotransferase_deficiency wasDerivedFrom Ornithine_aminotransferase_deficiency?oldid=692921500.
- Ornithine_aminotransferase_deficiency depiction L-Ornithine_structure.svg.
- Ornithine_aminotransferase_deficiency isPrimaryTopicOf Ornithine_aminotransferase_deficiency.
- Ornithine_aminotransferase_deficiency name "Ornithine aminotransferase deficiency".