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:
ACTH-dependent Cushing syndrome ACTH-independent Cushing syndrome Adrenal Cushing syndrome Adrenocortical carcinoma Alström syndrome Anaplastic thyroid carcinoma Antisynthetase syndrome Atypical hemolytic uremic syndrome Atypical hemolytic uremic syndrome with B factor anomaly Atypical hemolytic uremic syndrome with C3 anomaly Atypical hemolytic uremic syndrome with H factor anomaly Atypical hemolytic uremic syndrome with I factor anomaly Atypical hemolytic uremic syndrome with MCP/CD46 anomaly Atypical hemolytic uremic syndrome with anti-factor H antibodies Atypical hemolytic uremic syndrome with thrombomodulin anomaly Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Autoimmune interstitial lung disease-arthritis syndrome Autosomal systemic lupus erythematosus Bartter syndrome Basement membrane disease Behçet disease Congenital renal artery stenosis Cranioectodermal dysplasia Cushing disease Cushing syndrome due to bilateral macronodular adrenocortical disease Cushing syndrome due to ectopic ACTH secretion Cystinuria Cystinuria type A Cystinuria type B Dent disease Dermatomyositis Differentiated thyroid carcinoma Dominant hypophosphatemia with nephrolithiasis or osteoporosis EAST syndrome Endogenous Cushing syndrome Fabry disease Familial nonmedullary thyroid carcinoma Familial papillary thyroid carcinoma with renal papillary neoplasia Familial primary hyperparathyroidism Genetic cystic renal disease Genetic hyperparathyroidism Genetic primary hypomagnesemia Genetic renal tubular disease Giant cell arteritis Gitelman syndrome Glomerular disease Granulomatosis with polyangiitis HNF1B-related autosomal dominant tubulointerstitial kidney disease Hemolytic uremic syndrome with DGKE deficiency Hereditary renal hypouricemia Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome Hypophosphatemic rickets Hypotonia-cystinuria type 1 syndrome Idiopathic hypercalciuria IgG4-related disease IgG4-related kidney disease IgG4-related retroperitoneal fibrosis Jeune syndrome Joubert syndrome with oculorenal defect Juvenile dermatomyositis Juvenile polymyositis Medullary thyroid carcinoma Microscopic polyangiitis Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Mixed connective tissue disease Multiple endocrine neoplasia Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Multiple endocrine neoplasia type 4 Nail-patella syndrome Neonatal severe primary hyperparathyroidism Nephrogenic diabetes insipidus Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome Nephrogenic syndrome of inappropriate antidiuresis Nephronophthisis Nephropathy secondary to a storage or other metabolic disease Oculocerebrorenal syndrome of Lowe Overlapping connective tissue disease PLCG2-associated antibody deficiency and immune dysregulation Pediatric systemic lupus erythematosus Polymyositis Predominantly large-vessel vasculitis Predominantly medium-vessel vasculitis Predominantly small-vessel vasculitis Primary Fanconi renotubular syndrome Primary glomerular disease Primary renal tubular acidosis Prolactinoma Pseudohypoaldosteronism Pseudohypoparathyroidism REN-related autosomal dominant tubulointerstitial kidney disease RHYNS syndrome Rare cause of hypertension Rare disease with adrenal Cushing syndrome as a major feature Rare genetic cause of hypertension Rare renal tubular disease Rare thyroid carcinoma Relapsing polychondritis Reynolds syndrome STAT3-related early-onset multisystem autoimmune disease Saldino-Mainzer syndrome Sarcoidosis Satoyoshi syndrome Secondary glomerular disease Secondary neonatal autoimmune disease Secondary vasculitis Senior-Boichis syndrome Senior-Loken syndrome Shiga toxin-associated hemolytic uremic syndrome Simple cryoglobulinemia Sjögren-Larsson syndrome Susac syndrome Syndromic multisystem autoimmune disease due to Itch deficiency Systemic autoimmune disease Systemic sclerosis Takayasu arteritis Thrombotic microangiopathy Tubulointerstitial nephritis and uveitis syndrome Unclassified vasculitis Undifferentiated connective tissue syndrome VIPoma Vasculitis