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