Unstable hemoglobin disease
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Klinik und Poliklinik für Pädiatrische Hämatologie und Onkologie am Universitätsklinikum Hamburg-Eppendorf
Martin Zeitz Centrum für Seltene Erkrankungen (MZCSE) Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741054270
040 741054601
Website
Email
- Combined T and B cell immunodeficiency
- Medulloblastoma
- Fanconi anemia
- Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome
- Sickle cell anemia
- Rhabdomyosarcoma
- Congenital factor V deficiency
- Alveolar soft tissue sarcoma
- Alpha-thalassemia
- Hemophilia
- Beta-thalassemia
- Von Willebrand disease
- Retinoblastoma
Pädiatrie 5 – Onkologie, Hämatologie und Immunologie am Klinikum Stuttgart
Klinikum Stuttgart
Kriegsbergstraße 62
70174 Stuttgart
0711 27872461
0711 27872462
Website
Email
Zentrum für Seltene Störungen der Hämatopoese und Immundefekte (ZSHI) am Universitätsklinikum Ulm
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstrasse 24
89075 Ulm
- Hereditary spherocytosis
- Quantitative and/or qualitative congenital phagocyte defect
- Paroxysmal nocturnal hemoglobinuria
- Severe combined immunodeficiency
- Rare anemia
- Polycythemia
- Primary immunodeficiency due to a defect in innate immunity
- Alpha-thalassemia
- Beta-thalassemia
- Sickle cell anemia
- Immunodeficiency predominantly affecting antibody production
- Autoimmune thrombocytopenia
- Syndrome with combined immunodeficiency
- Autoinflammatory syndrome of childhood
- Immune dysregulation disease with immunodeficiency
Zentrum für angeborene Blutzellerkrankungen am Universitätsklinikum Würzburg
Zentrum für Seltene Erkrankungen - Referenzzentrum Nordbayern (ZESE) Universitätsklinikum Würzburg
Josef-Schneider-Straße 2
97080 Würzburg
- Hemoglobinopathy
- Hereditary spherocytosis
- Sickle cell anemia
- Hereditary stomatocytosis
- Fanconi anemia
- Hermansky-Pudlak syndrome
- Congenital dyserythropoietic anemia
- Beta-thalassemia and related diseases
- Alpha-thalassemia
- Bernard-Soulier syndrome
- Glanzmann thrombasthenia
- Class I glucose-6-phosphate dehydrogenase deficiency
- MYH9-related disease
- Alpha-thalassemia and related disorders
- Hemolytic anemia due to red cell pyruvate kinase deficiency