Hereditary stomatocytosis
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Klinik für Kinder und Jugendmedizin- Pädiatrische Hämatologie & Onkologie am Universitätsklinikum Münster
Centrum für seltene Erkrankungen Münster Universitätsklinikum Münster (UKM)
Albert-Schweitzer-Campus 1
48149 Münster
0251 8347742
0251 8347828
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Zentrum für Seltene Störungen der Hämatopoese und Immundefekte (ZSHI) am Universitätsklinikum Ulm
Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm Universitätsklinikum Ulm
Eythstrasse 24
89075 Ulm
- Paroxysmal nocturnal hemoglobinuria
- Immune dysregulation disease with immunodeficiency
- Quantitative and/or qualitative congenital phagocyte defect
- Autoinflammatory syndrome of childhood
- Syndrome with combined immunodeficiency
- Autoimmune thrombocytopenia
- Immunodeficiency predominantly affecting antibody production
- Sickle cell anemia
- Primary immunodeficiency due to a defect in innate immunity
- Polycythemia
- Beta-thalassemia
- Hereditary spherocytosis
- Alpha-thalassemia
- Severe combined immunodeficiency
- Rare anemia
Zentrum für angeborene Blutzellerkrankungen am Universitätsklinikum Würzburg
Universitätsklinikum Würzburg Zentrum für Seltene Erkrankungen - Referenzzentrum Nordbayern (ZESE)
Josef-Schneider-Straße 2
97080 Würzburg
- Alpha-thalassemia
- Sickle cell anemia
- Hereditary stomatocytosis
- Fanconi anemia
- Congenital dyserythropoietic anemia
- Hereditary spherocytosis
- Alpha-thalassemia and related disorders
- Bernard-Soulier syndrome
- Hermansky-Pudlak syndrome
- Hemoglobinopathy
- MYH9-related disease
- Beta-thalassemia and related diseases
- Class I glucose-6-phosphate dehydrogenase deficiency
- Glanzmann thrombasthenia
- Hemolytic anemia due to red cell pyruvate kinase deficiency