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