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