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Browse Symptoms, Findings, Diseases & Conditions > Disease Information > Disease Processes > Metabolic-Storage > Major Organs-Systems > Pediatric
- 237 related diseases found
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- Disease Information
- Disease Processes
- Metabolic-Storage
- Major Organs-Systems
- Pediatric
- Abetalipoproteinemia (Bassen Kornzweig) - Disease Information
- Acatalasia - Disease Information
- Acid phosphatase, lysosomal, deficiency - Disease Information
- Acrodermatitis enteropathica - Disease Information
- Acyl-CoA Dehydrogenase/short chain def - Disease Information
- Adenosine deaminase defic/SCID variant - Disease Information
- Adenosine diaminase excess RBC's - Disease Information
- Adenyl succinate lysate deficiency - Disease Information
- Adrenogenital syndrome - Disease Information
- Adult amaurotic familial idiocy - Disease Information
- Albinism - Disease Information
- Alkaptonuria/Ochronosis - Disease Information
- Alphamethylacetoacetate accumulation - Disease Information
- Aminoacid enzyme/metabolic disorder - Disease Information
- Aminoaciduria - Disease Information
- Amyloidosis, hereditofamilial - Disease Information
- Amylopectinosis (Andersen's) disease (GSD IV) - Disease Information
- Analbuminemia - Disease Information
- Anemia due to glutathione metab def - Disease Information
- Aspartylglycosaminuria - Disease Information
- Barth Syndrome/3 MethylGlutoconic aciduria/MGA II - Disease Information
- Beta-alaninemia - Disease Information
- Beta-glucuronidase deficiency syndrome (MPS VII) - Disease Information
- Beta-hydroxyisolvaleric acidemia - Disease Information
- Biber-Haab-Dimmer syndrome - Disease Information
- Carbamoyl phosphate synthetase defic - Disease Information
- Carbohydrate malabsorption, subclinical - Disease Information
- Carbonic anhydrase I deficiency - Disease Information
- Carnitine deficiency syndrome - Disease Information
- Carnitine/Acylcarnitine translocase deficiency - Disease Information
- Carnosinemia - Disease Information
- Cerebral Gaucher's of infants (acute) - Disease Information
- Cerebral glycogen storage/GSD VIII - Disease Information
- Citrullinemia/Argininsuccinicaciduria - Disease Information
- Citrullinuria - Disease Information
- Combined carboxylase/Biotinidase deficiency - Disease Information
- Congenital cholinesterase deficiency - Disease Information
- Congenital erythropoetic porphyria - Disease Information
- Congenital hypophosphatasia - Disease Information
- Coproporphyria erythrohepatica - Disease Information
- Coproporphyria, hereditary - Disease Information
- Corticosterone methyl oxidase defic'y - Disease Information
- Crigler-Najjar syndrome - Disease Information
- Cystathioninuria - Disease Information
- Cystic fibrosis (mucoviscidosis) - Disease Information
- Cystinosis - Disease Information
- Cystinosis, adolescent - Disease Information
- Cystinuria - Disease Information
- Cytochrome C Oxidase Deficiency/COX Complex Defect - Disease Information
- Diabetes mellitus/juvenile (Type I) - Disease Information
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