Hereditary stomatocytosis
Parent facilities 0
Genetic Advices 0
Care facilities 4
Klinik für Pädiatrische Hämatologie und Onkologie am Universitätsklinikum Freiburg
Universitätsklinikum Freiburg
Mathildenstraße 1
79106 Freiburg
0761 27045200
0761 27043010
Website
Email
- Hemoglobinopathy
- Rare lymphatic malformation
- Beta-thalassemia
- Chronic myelomonocytic leukemia
- Von Willebrand disease
- Rare hemolytic anemia
- Rare venous malformation
- Diamond-Blackfan anemia
- Juvenile myelomonocytic leukemia
- Congenital factor XI deficiency
- Rare capillary malformation
- Rare aplastic anemia
- Paroxysmal nocturnal hemoglobinuria
- Myelodysplastic syndrome
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
Website
Email
Zentrum für Seltene Störungen der Hämatopoese und Immundefekte (ZSHI) am Universitätsklinikum Ulm
Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm Universitätsklinikum Ulm
Eythstrasse 24
89075 Ulm
- Rare anemia
- Autoimmune thrombocytopenia
- Severe combined immunodeficiency
- Hereditary spherocytosis
- Sickle cell anemia
- Beta-thalassemia
- Polycythemia
- Alpha-thalassemia
- Autoinflammatory syndrome of childhood
- Syndrome with combined immunodeficiency
- Immunodeficiency predominantly affecting antibody production
- Paroxysmal nocturnal hemoglobinuria
- Immune dysregulation disease with immunodeficiency
- Primary immunodeficiency due to a defect in innate immunity
- Quantitative and/or qualitative congenital phagocyte defect
Zentrum für angeborene Blutzellerkrankungen am Universitätsklinikum Würzburg
Universitätsklinikum Würzburg Zentrum für Seltene Erkrankungen - Referenzzentrum Nordbayern (ZESE)
Josef-Schneider-Straße 2
97080 Würzburg
- Beta-thalassemia and related diseases
- Alpha-thalassemia
- Hemolytic anemia due to red cell pyruvate kinase deficiency
- Congenital dyserythropoietic anemia
- Bernard-Soulier syndrome
- Hermansky-Pudlak syndrome
- Sickle cell anemia
- Fanconi anemia
- Class I glucose-6-phosphate dehydrogenase deficiency
- Hemoglobinopathy
- Hereditary spherocytosis
- Glanzmann thrombasthenia
- Alpha-thalassemia and related disorders
- Hereditary stomatocytosis
- MYH9-related disease