Fatal infantile lactic acidosis with methylmalonic aciduria
Parent facilities 0
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Zentrum für angeborene Stoffwechselerkrankungen am Universitätsklinikum Freiburg
Freiburg Zentrum für Seltene Erkrankungen (FZSE) Universitätsklinikum Freiburg
Breisacherstr. 62
79106 Freiburg
- Maple syrup urine disease
- Disorder of ketolysis
- Disorder of branched-chain amino acid metabolism
- Disorder of galactose metabolism
- Gluconeogenesis disorder
- Disorder of fatty acid oxidation and ketone body metabolism
- Disorder of fructose metabolism
- Hereditary fructose intolerance
- Glycogen storage disease
- Glucose-galactose malabsorption
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Zentrum für seltene Stoffwechselerkrankungen der Medizinischen Hochschule Hannover
Zentrum für Seltene Erkrankungen Hannover Medizinische Hochschule Hannover
Carl-Neuberg-Straße 1
30625 Hannover
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
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Email
- Infantile neuroaxonal dystrophy
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Rare ataxia
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Atypical pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
- Leukodystrophy
- Hereditary spastic paraplegia
- Neuroferritinopathy
- Mitochondrial membrane protein-associated neurodegeneration
Zentrum für angeborene pädiatrische Stoffwechselerkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum Care for Rare Center am Dr. von Haunerschen Kinderspital am LMU Klinikum München
Lindwurmstr. 4
80337 München
- Glycogen storage disease
- Very long chain acyl-CoA dehydrogenase deficiency
- Phenylketonuria
- Maple syrup urine disease
- Disorder of carnitine cycle and carnitine transport
- Disorder of urea cycle metabolism and ammonia detoxification
- Glutaryl-CoA dehydrogenase deficiency
- Mitochondrial disease
- Fabry disease
- Tyrosinemia type 1
- Medium chain acyl-CoA dehydrogenase deficiency
- Galactosemia
Zentrum für metabolische Erkrankungen (ZME)-Tübingen
Paul-Ehrlich-Strasse 23
72076 Tübingen
070717049000
070717049002
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