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