Association for Glycogen Storage Disease, UK

All you need to know about BH4.

Children living with inherited metabolic diseases

Cochrane Cystic Fibrosis and Genetic Disorders Group

Congenital Disorders of Glycosylation (CDG)

Databases of Pediatric Neurotransmitter Disorders inc. PKU

European Directory of DNA Laboratories

Fatty Oxidation Disorders (FOD) Family Support Group

Foundation for the Study of Infant Deaths

Gauchers Association, UK

KUMC Genetics Education Center

Lysosomal Storage Research
A multimedia virtual clinic applied specifically to mucopolysaccharidosis type II (MPS II, Hunter disease)

Metab-L Mailing List

Mitochondria Research Society

Mitochondrial Medicine Society (MMS)

National Metabolic Biochemistry Network

National Niemann-Pick Disease Foundation

National Organization for Rare Disorders (NORD)

National Society for Phenylketonuria

OMIM -- Online Mendelian Inheritance in Man

Organic Acidemia Association

Orphan Europe Academy

ORPHANET is a database dedicated to information on rare diseases and orphan drugs.

Pediatric Neurotransmitter Disease Association

PKU Academy
PKU Academy presents invaluable opportunities to learn about PKU through many educational resources and online programs. In the Academy section of the website, healthcare professionals can access e-learning courses containing basic information about phenylketonuria. Users also have access to a glossary of important terminology in PKU, a calendar of events and links to international societies dedicated to inherited metabolic disorders.

PKU World Link

The Children's Mitchondrial Disease Network

The Pompe's Disease Page

The Society for Mucopolysaccharide Diseases Home Page

United Mitochondrial Disease Foundation


Membership of the Society is open to all interested in and willing to support the aims of the Society.

 Membership 2020      User Profile


SSIEM Administrator

Society for the Study of Inborn
Errors of Metabolism (SSIEM)
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London SE1 2TU

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Journal of Inherited Metabolic Disease

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