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