SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
Autoimmune pancreatitis Congenital disorder of glycosylation Congenital pancreatic cyst Disorder of amino acid absorption and transport Disorder of amino acid and other organic acid metabolism Disorder of asparagine metabolism Disorder of beta and omega amino acid metabolism Disorder of biogenic amine metabolism and transport Disorder of branched-chain amino acid metabolism Disorder of carbohydrate metabolism Disorder of energy metabolism Disorder of glutamine metabolism Disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation Disorder of histidine metabolism Disorder of lipid absorption and transport Disorder of lipid metabolism Disorder of lysine and hydroxylysine metabolism Disorder of lysosomal amino acid transport Disorder of lysosomal-related organelles Disorder of metabolite absorption and transport Disorder of methionine cycle and sulfur amino acid metabolism Disorder of multiple glycosylation Disorder of ornithine or proline metabolism Disorder of peptide metabolism Disorder of phenylalanin or tyrosine metabolism Disorder of porphyrin and heme metabolism Disorder of protein N-glycosylation Disorder of protein O-glycosylation Disorder of purine or pyrimidine metabolism Disorder of serine or glycine metabolism Disorder of sialic acid metabolism Disorder of the gamma-glutamyl cycle Disorder of tryptophan metabolism Disorder of urea cycle metabolism and ammonia detoxification Follicular cholangitis and pancreatitis Glycoproteinosis Hepatocellular carcinoma Hereditary chronic pancreatitis Infantile multisystem neurologic-endocrine-pancreatic disease Lipid storage disease Lysosomal acid phosphatase deficiency Lysosomal disease Lysosomal glycogen storage disease Mucolipidosis Mucopolysaccharidosis Neuronal ceroid lipofuscinosis Oligosaccharidosis Organic aciduria Other metabolic disease Pancreatic insufficiency-anemia-hyperostosis syndrome Peroxisomal disease Primary sclerosing cholangitis Pycnodysostosis Rare hereditary hemochromatosis Rare inborn errors of metabolism Rare pancreatic disease Rare tumor of pancreas Recurrent acute pancreatitis Reynolds syndrome Shwachman-Diamond syndrome Sphingolipidosis Tropical pancreatitis Wilson disease