V. Medizinische Klinik der Universitätsmedizin Mannheim Assigned 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