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
- Hemoglobinopathy
- Von Willebrand disease
- Rare capillary malformation
- Beta-thalassemia
- Diamond-Blackfan anemia
- Paroxysmal nocturnal hemoglobinuria
- Myelodysplastic syndrome
- Rare aplastic anemia
- Rare lymphatic malformation
- Chronic myelomonocytic leukemia
- Rare hemolytic anemia
- Juvenile myelomonocytic leukemia
- Rare venous malformation
- Congenital factor XI deficiency
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
- Alpha-thalassemia
- Autoinflammatory syndrome of childhood
- Syndrome with combined immunodeficiency
- Primary immunodeficiency due to a defect in innate immunity
- Beta-thalassemia
- Polycythemia
- Rare anemia
- Hereditary spherocytosis
- Severe combined immunodeficiency
- Paroxysmal nocturnal hemoglobinuria
- Sickle cell anemia
- Immunodeficiency predominantly affecting antibody production
- Immune dysregulation disease with immunodeficiency
- Autoimmune thrombocytopenia
- 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
- Hereditary spherocytosis
- Alpha-thalassemia and related disorders
- Hermansky-Pudlak syndrome
- MYH9-related disease
- Class I glucose-6-phosphate dehydrogenase deficiency
- Glanzmann thrombasthenia
- Fanconi anemia
- Sickle cell anemia
- Beta-thalassemia and related diseases
- Bernard-Soulier syndrome
- Hemoglobinopathy
- Congenital dyserythropoietic anemia
- Alpha-thalassemia
- Hemolytic anemia due to red cell pyruvate kinase deficiency
- Hereditary stomatocytosis