Metabolic Disorders

Article describes the disorder, its symptoms, diagnosis, and treatment. From the About.com Guide to Rare/Orphan Diseases.

Article explains the disease, its symptoms, diagnosis, and treatments, and what new therapies are being explored. From the About.com Guide to Rare/Orphan Diseases.

Article describes Crigler-Najjar syndrome, its symptoms, diagnosis, and treatment.

Article describes cystinuria, its symptoms, diagnosis, and treatment.

Article describes Hartnup disease, its symptoms, diagnosis, and treatment.

Information about the inherited metabolic disorder histidinemia, including symptoms, diagnosis, and treatment.

Article describes maple syrup urine disease, its symptoms, diagnosis, and treatment.

Article describes Menkes kinky hair disease, its symptoms, diagnosis, and treatment. From the About.com Guide to Rare/Orphan Diseases.

Information about phenylketonuria (PKU), an inherited metabolic disorder, including symptoms, testing, diagnosis, and treatment.

Article describes sitosterolemia, its symptoms, diagnosis, and treatment.

Article describes Smith-Lemli-Opitz syndrome, its symptoms, diagnosis, and treatment.

Article describes the disorder, its symptoms, diagnosis, and treatment. From the About.com Guide to Rare/Orphan Diseases.

Article describes the urea cycle disorders, their diagnosis, and treatment. From the About.com Guide to Rare/Orphan Diseases.

Information about Wilson's disease, an inherited genetic disorder of copper metabolism, including symptoms, diagnosis, and treatment.

Article describes Zellweger syndrome, its symptoms, diagnosis, and treatment.

Climb is committed to fighting metabolic diseases through research, awareness and support. We are the UK's only dedicated organisation to provide advice, information and support on all metabolic diseases to children, young adults, families, carers and professionals.