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