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