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