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tyrosinemia type ii
(phenotype)
Summary
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
TAT
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
Tyrosine aminotransferase
Tyrosine/nicotianamine aminotransferase
Tyrosine aminotransferase ubiquitination region
Aminotransferases, class-I, pyridoxal-phosphate-binding site
Aminotransferase, class I/classII
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OMIM - Congenital disorder
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Literature
Most Relevant Literature
Bilateral recurrent pseudodendritic keratopathy as the initial manifestation of tyrosinemia type II.
Omega-3 fatty acid supplementation decreases DNA damage in brain of rats subjected to a chemically i…
Tyrosinemia type II: novel mutations in the TAT gene in a boy with unusual presentation.
Role of antioxidant treatment on DNA and lipid damage in the brain of rats subjected to a chemically…
Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects w…
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Clinical Trials
Most Relevant Clinical Trials
Phase II Study of the Enzyme Inhibitor NTBC for Tyrosinemia Type I
Study of NTBC for Tyrosinemia I
Evaluation of TYR Sphere
Selective Screening of Children for Hereditary Metabolic Diseases by Tandem Mass Spectrometry in Kaz…
Baby Detect : Genomic Newborn Screening
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