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