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
- Beta-thalassemia
- Von Willebrand disease
- Diamond-Blackfan anemia
- Rare lymphatic malformation
- Rare hemolytic anemia
- Chronic myelomonocytic leukemia
- Rare venous malformation
- Rare capillary malformation
- Rare aplastic anemia
- Congenital factor XI deficiency
- Juvenile myelomonocytic leukemia
- Myelodysplastic syndrome
- Paroxysmal nocturnal hemoglobinuria
Klinik für Kinder und Jugendmedizin- Pädiatrische Hämatologie & Onkologie am Universitätsklinikum Münster
Universitätsklinikum Münster (UKM) Centrum für seltene Erkrankungen Münster
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
- 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
Zentrum für Seltene Erkrankungen - Referenzzentrum Nordbayern (ZESE) Universitätsklinikum Würzburg
Josef-Schneider-Straße 2
97080 Würzburg
- Hereditary stomatocytosis
- Fanconi anemia
- MYH9-related disease
- Sickle cell anemia
- Hemoglobinopathy
- Class I glucose-6-phosphate dehydrogenase deficiency
- Congenital dyserythropoietic anemia
- Alpha-thalassemia
- Hereditary spherocytosis
- Glanzmann thrombasthenia
- Bernard-Soulier syndrome
- Hermansky-Pudlak syndrome
- Hemolytic anemia due to red cell pyruvate kinase deficiency
- Alpha-thalassemia and related disorders
- Beta-thalassemia and related diseases