Metabolic Support UK
Unit 11-12 Gwenfro
Wrexham, Wales
01244-207581 or 0845-241-2173
About Metabolic Support UK
CLIMB (Children Living with Inherited Metabolic Diseases) is an international, voluntary health agency located in the United Kingdom and is also the National Information and Advice Centre for Metabolic Diseases. Established in 1981, it is dedicated to furthering medical research into the nature of metabolic diseases in children; encouraging the ongoing investigations of the prenatal diagnosis of these diseases; providing information, advice and support to caregivers; providing limited financial support grants; and providing information to healthcare professionals. In addition, the organization assists in the care of affected children in hospitals, homes or institutions and educates the public about metabolic diseases. CLIMB networks parents of affected children for mutual benefit and support. It also provides a regular newsletter, brochures, videos and other educational materials.
Related Rare Diseases:
- Glucose-Galactose Malabsorption
- Sandhoff Disease
- Aromatic L-Amino Acid Decarboxylase Deficiency
- Propionic Acidemia
- Menkes Disease
- Primary Mitochondrial Myopathies
- Mucopolysaccharidosis Type I
- Arginine: Glycine Amidinotransferase Deficiency
- Guanidinoacetate Methyltransferase Deficiency
- Creatine Transporter Deficiency
- Carnosinemia
- Cerebral Creatine Deficiency Syndromes
- TANGO2-Related Metabolic Encephalopathy and Arrhythmias
- Hereditary Orotic Aciduria
- Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation
- Pycnodysostosis
- Hajdu Cheney Syndrome
- Classic Infantile CLN1 Disease
- Acid Sphingomyelinase Deficiency
- Sepiapterin Reductase Deficiency
- Bile Acid Synthesis Disorders
- Dent Disease
- Hepatoerythropoietic Porphyria
- Centronuclear Myopathy
- X-Linked Protoporphyria
- Familial Partial Lipodystrophy
- Congenital Generalized Lipodystrophy
- Congenital Disorders of Glycosylation
- Glucose Transporter Type 1 Deficiency Syndrome
- Lysosomal Free Sialic Acid Storage Disorders
- Wolman Disease
- Triosephosphate Isomerase Deficiency
- Cerebrotendinous Xanthomatosis
- Maternally Inherited Leigh Syndrome and NARP Syndrome
- Lysosomal Storage Disorders
- Barth Syndrome
- Fucosidosis
- Cytochrome C Oxidase Deficiency
- Crigler Najjar Syndrome
- PMM2-CDG
- Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)
- Schindler disease
- Trimethylaminuria
- X-Linked Myotubular Myopathy
- MERRF Syndrome
- MELAS Syndrome
- Aspartylglycosaminuria
- Carnitine Palmitoyltransferase 1A Deficiency
- Phosphoglycerate Kinase Deficiency
- Pyruvate Carboxylase Deficiency
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Hypokalemia
- Valinemia
- Congenital Sucrase-Isomaltase Deficiency
- Histidinemia
- Medium Chain Acyl CoA Dehydrogenase Deficiency
- Hyperprolinemia Type I
- Hyperprolinemia Type II
- Multiple Sulfatase Deficiency
- Glutathione Synthetase Deficiency
- Nonketotic Hyperglycinemia
- Hypophosphatasia
- Acrodermatitis Enteropathica
- Isovaleric Acidemia
- Biotinidase Deficiency
- Familial Lipoprotein Lipase Deficiency
- Primary Hyperoxaluria
- Homocystinuria due to Cystathionine Beta-Synthase Deficiency
- Acquired Lipodystrophy
- Tyrosinemia Type 1
- Tetrahydrobiopterin Deficiency
- Alpha-Mannosidosis
- Pyruvate Dehydrogenase Complex Deficiency
- Pompe Disease
- Glycogen Storage Disease Type VI
- Glycogen Storage Disease Type IX
- Glycogen Storage Disease Type 7
- Glycogen Storage Disease Type III
- Glycogen Storage Disease Type V
- Andersen Disease (GSD IV)
- Glycogen Storage Disease Type I
- Leigh Syndrome
- Leprechaunism
- Glutaric Aciduria Type I
- Leukodystrophy
- Glutaric Aciduria Type II
- Galactosemia
- Osteopetrosis
- Refsum Disease
- Hartnup Disease
- Variegate Porphyria
- Hereditary Coproporphyria
- Erythropoietic Protoporphyria and X-Linked Protoporphyria
- ALAD Porphyria
- Acute Intermittent Porphyria
- N-Acetylglutamate Synthetase Deficiency
- Arginase-1 Deficiency
- Argininosuccinic Aciduria
- Citrullinemia Type 1
- Ornithine Transcarbamylase Deficiency
- Carbamoyl Phosphate Synthetase 1 Deficiency
- I Cell Disease
- Pseudo Hurler Polydystrophy
- Sialidosis
- Mucopolysaccharidosis IV
- Mucopolysaccharidosis Type VII
- Mucopolysaccharidosis Type III
- Maroteaux Lamy Syndrome
- Mucopolysaccharidosis Type II
- Juvenile CLN3 Disease
- Lesch Nyhan Syndrome
- Fabry Disease
- Pantothenate Kinase-Associated Neurodegeneration
- Cockayne Syndrome
- Blue Diaper Syndrome
- Pelizaeus-Merzbacher Disease
- Maple Syrup Urine Disease
- Congenital Adrenal Hyperplasia
- Niemann Pick Disease Type C
- Systemic Primary Carnitine Deficiency
- Cystinosis
- Alkaptonuria
- Tay Sachs Disease
- Síndrome de deficiencia del transportador de glucosa tipo 1
- Trastornos congénitos de la glicosilación (2021)
- Pseudohypoparathyroidism
