Tyrosinaemia-tyrosiluria hereditary syndrome

disorder

SNOMED 271847005CUI C0268486

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Treatments & Interventions

Hemin

substance

Ascorbic acid

substance

Sodium ascorbate

substance

Nitisinone

substance

Related Conditions

Tyrosinaemia type I(child)

Fumarylacetoacetase deficiency, chronic type(child)

Hypertyrosinemia, Richner-Hanhart type(child)

Hypertyrosinemia(parent)

Hereditary metabolic disease(parent)

Quick Facts

SNOMED CT: 271847005
UMLS CUI: C0268486
Fully Specified Name: Hereditary hypertyrosinemia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
Known Treatments: 4

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.