Glycogen storage disease due to phosphoglycerate mutase deficiency
All Entries 8
Klinik für Neurologie am St. Josefs Hospital Bochum
St. Josefs Hospital - Katholisches Klinikum Bochum
Gudrunstraße 56
44791 Bochum
0234 5092420
0234 5092414
Website
Email
Universitäts NeuroMuskuläres Centrum am Universitätsklinikum Dresden
Universitätsklinikum Carl Gustav Carus Dresden UniversitätsCentrum für Seltene Erkrankungen Dresden (USE)
Fetscherstr. 74
01307 Dresden
0351 4583876
0351 4585802
Website
- Juvenile myasthenia gravis
- Dermatomyositis
- Limb-girdle muscular dystrophy
- Guillain-Barré syndrome
- Lambert-Eaton myasthenic syndrome
- Amyotrophic lateral sclerosis
- Myotonic dystrophy
- Charcot-Marie-Tooth disease type 1
- Rhabdomyosarcoma
- Malignant hyperthermia of anesthesia
- Duchenne and Becker muscular dystrophy
- Botulism
Zentrum für angeborene Stoffwechselerkrankungen am Universitätsklinikum Freiburg
Freiburg Zentrum für Seltene Erkrankungen (FZSE) Universitätsklinikum Freiburg
Breisacherstr. 62
79106 Freiburg
- Hereditary fructose intolerance
- Disorder of fructose metabolism
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
- Disorder of branched-chain amino acid metabolism
- Glucose-galactose malabsorption
- Maple syrup urine disease
- Disorder of ketolysis
- Glycogen storage disease
- Disorder of galactose metabolism
- Disorder of fatty acid oxidation and ketone body metabolism
- Gluconeogenesis disorder
Zentrum für seltene Stoffwechselerkrankungen der Medizinischen Hochschule Hannover
Medizinische Hochschule Hannover Zentrum für Seltene Erkrankungen Hannover
Carl-Neuberg-Straße 1
30625 Hannover
Zentrum für angeborene pädiatrische Stoffwechselerkrankungen am LMU Klinikum München
Care for Rare Center am Dr. von Haunerschen Kinderspital am LMU Klinikum München Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
Lindwurmstr. 4
80337 München
- Disorder of carnitine cycle and carnitine transport
- Fabry disease
- Mitochondrial disease
- Phenylketonuria
- Glutaryl-CoA dehydrogenase deficiency
- Very long chain acyl-CoA dehydrogenase deficiency
- Tyrosinemia type 1
- Medium chain acyl-CoA dehydrogenase deficiency
- Galactosemia
- Glycogen storage disease
- Disorder of urea cycle metabolism and ammonia detoxification
- Maple syrup urine disease
Klinik für Kinder- und Jugendmedizin - Allgemeine Pädiatrie am Universitätsklinikum Münster
Centrum für seltene Erkrankungen Münster Universitätsklinikum Münster (UKM)
Albert-Schweitzer-Campus 1
48149 Münster
0251 8347732
0251 8347735
Website
Email
- Disorder of lipid metabolism
- Rare epilepsy
- Respiratory malformation
- Primary ciliary dyskinesia
- Autosomal dominant polycystic kidney disease
- Cystic fibrosis
- Disorder of carbohydrate metabolism
- Nephronophthisis
- Autosomal recessive polycystic kidney disease
- Disorder of amino acid and other organic acid metabolism
Glykogenose Deutschland e.V.
Post Office Box Am Römerweg 33e
55270
Essenheim
Deutsche Muskelschwund-Hilfe e.V. (DMH)
Alstertor 20
20095
Hamburg
- Bethlem muscular dystrophy
- Juvenile amyotrophic lateral sclerosis
- Amyotrophic lateral sclerosis
- Autosomal dominant limb-girdle muscular dystrophy
- Adult-onset distal myopathy due to VCP mutation
- Duchenne and Becker muscular dystrophy
- Myasthenia gravis
- Motor neuron disease
- Muscular channelopathy
- Neuromuscular junction disease
- BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy
- Finnish upper limb-onset distal myopathy
- Amyotrophic lateral sclerosis type 4
- Muscular dystrophy
- Neuromuscular disease
Parent facilities 0
Genetic Advices 0
Care facilities 6
Klinik für Neurologie am St. Josefs Hospital Bochum
St. Josefs Hospital - Katholisches Klinikum Bochum
Gudrunstraße 56
44791 Bochum
0234 5092420
0234 5092414
Website
Email
Universitäts NeuroMuskuläres Centrum am Universitätsklinikum Dresden
Universitätsklinikum Carl Gustav Carus Dresden UniversitätsCentrum für Seltene Erkrankungen Dresden (USE)
Fetscherstr. 74
01307 Dresden
0351 4583876
0351 4585802
Website
- Juvenile myasthenia gravis
- Dermatomyositis
- Limb-girdle muscular dystrophy
- Guillain-Barré syndrome
- Lambert-Eaton myasthenic syndrome
- Amyotrophic lateral sclerosis
- Myotonic dystrophy
- Charcot-Marie-Tooth disease type 1
- Rhabdomyosarcoma
- Malignant hyperthermia of anesthesia
- Duchenne and Becker muscular dystrophy
- Botulism
Zentrum für angeborene Stoffwechselerkrankungen am Universitätsklinikum Freiburg
Freiburg Zentrum für Seltene Erkrankungen (FZSE) Universitätsklinikum Freiburg
Breisacherstr. 62
79106 Freiburg
- Hereditary fructose intolerance
- Disorder of fructose metabolism
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
- Disorder of branched-chain amino acid metabolism
- Glucose-galactose malabsorption
- Maple syrup urine disease
- Disorder of ketolysis
- Glycogen storage disease
- Disorder of galactose metabolism
- Disorder of fatty acid oxidation and ketone body metabolism
- Gluconeogenesis disorder
Zentrum für seltene Stoffwechselerkrankungen der Medizinischen Hochschule Hannover
Medizinische Hochschule Hannover Zentrum für Seltene Erkrankungen Hannover
Carl-Neuberg-Straße 1
30625 Hannover
Zentrum für angeborene pädiatrische Stoffwechselerkrankungen am LMU Klinikum München
Care for Rare Center am Dr. von Haunerschen Kinderspital am LMU Klinikum München Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
Lindwurmstr. 4
80337 München
- Disorder of carnitine cycle and carnitine transport
- Fabry disease
- Mitochondrial disease
- Phenylketonuria
- Glutaryl-CoA dehydrogenase deficiency
- Very long chain acyl-CoA dehydrogenase deficiency
- Tyrosinemia type 1
- Medium chain acyl-CoA dehydrogenase deficiency
- Galactosemia
- Glycogen storage disease
- Disorder of urea cycle metabolism and ammonia detoxification
- Maple syrup urine disease
Klinik für Kinder- und Jugendmedizin - Allgemeine Pädiatrie am Universitätsklinikum Münster
Centrum für seltene Erkrankungen Münster Universitätsklinikum Münster (UKM)
Albert-Schweitzer-Campus 1
48149 Münster
0251 8347732
0251 8347735
Website
Email
- Disorder of lipid metabolism
- Rare epilepsy
- Respiratory malformation
- Primary ciliary dyskinesia
- Autosomal dominant polycystic kidney disease
- Cystic fibrosis
- Disorder of carbohydrate metabolism
- Nephronophthisis
- Autosomal recessive polycystic kidney disease
- Disorder of amino acid and other organic acid metabolism
Supportgroups 2
Glykogenose Deutschland e.V.
Post Office Box Am Römerweg 33e
55270
Essenheim
Deutsche Muskelschwund-Hilfe e.V. (DMH)
Alstertor 20
20095
Hamburg
- Bethlem muscular dystrophy
- Juvenile amyotrophic lateral sclerosis
- Amyotrophic lateral sclerosis
- Autosomal dominant limb-girdle muscular dystrophy
- Adult-onset distal myopathy due to VCP mutation
- Duchenne and Becker muscular dystrophy
- Myasthenia gravis
- Motor neuron disease
- Muscular channelopathy
- Neuromuscular junction disease
- BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy
- Finnish upper limb-onset distal myopathy
- Amyotrophic lateral sclerosis type 4
- Muscular dystrophy
- Neuromuscular disease