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tyrosinemia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
GSTZ1
HPD
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
MODULE_78
MODULE_373
aromatic amino acid family metabolic process
MODULE_235
MODULE_40
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Most Correlated Studies
Mouse Phenotypes - Specific enzyme deficiency
Mouse Phenotypes - Autosomal dominant hereditary disorder
OMIM - Congenital disorder
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Literature
Most Relevant Literature
Neonatal hyperinsulinism in transient and classical forms of tyrosinemia.
Nitisinone treatment during two pregnancies and breastfeeding in a woman with tyrosinemia type 1 - a…
Determinants of tyrosinaemia during nitisinone therapy in alkaptonuria.
Evaluation of a New 'Mix-In' Style Glycomacropeptide-Based Protein Substitute for Food and Drinks in…
Syndrome of Inappropriate Antidiuretic Hormone Secretion in a Patient with Uncontrolled Tyrosinaemia…
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Clinical Trials
Most Relevant Clinical Trials
Biomarker for the Early Diagnosis and Monitoring in Tyrosinemia Type 1 (BioTyrosin)
Study of NTBC for Tyrosinemia I
Hereditary Hepatorenal Tyrosinemia Natural History in Egypt and the Arab World (Multicenter Clinical…
Phase II Study of the Enzyme Inhibitor NTBC for Tyrosinemia Type I
Bioavailability Food-Effect Study of an Oral Nitisinone Formulation to Treat Hereditary Tyrosinemia …
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