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