Children Living with Inherited Metabolic Diseases (CLIMB)

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Learn more about:
Acanthocytosis 3-methylcrotonyl-CoA carboxylase deficiency Homocystinuria due to defect in methylation cbl e Homocystinuria due to defect in methylation (cbl g) Homocystinuria X-linked adrenoleukodystrophy 2-methyl-3-hydroxybutyric aciduria Primary Hyperoxaluria Type 1 Primary carnitine deficiency
Related Access Program
University of Minnesota – Clinical and Translational Science Institute – X-linked Adrenoleukodystrophy

Climb is the leading patient organisation for Inherited Metabolic Disorders, supporting thousands of patients worldwide.

Climb Building 
176 Nantwich Road 
Crewe CW2 6BG 
United Kingdom 
Toll-free: 0800 652 3181 
Telephone: 0845 241 2173 
E-mail: [email protected]
Website: http://www.climb.org.uk