Tyrosinaemia Type 2
IMPORTANT INFORMATION
The information on the Rare Awareness Rare Education (RARE) Portal is intended for educational purposes only and does not replace professional advice.
Rare diseases typically display a high level of symptom complexity and variability. Individuals diagnosed with the same rare disease may be impacted differently and each person’s experience is unique. Please seek support from qualified healthcare professionals to learn more about the most suitable care and support options for you.
This page is currently under development. More information will be added in time.
For more information on this disease, please refer to:
- Metabolic Dietary Disorders Association (MDDA)
- Orphanet: Tyrosinemia type 2
- Genetic and Rare Diseases (GARD) Information Center: Tyrosinemia type 2
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