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
- Juvenile myelomonocytic leukemia
- Rare capillary malformation
- Rare aplastic anemia
- Paroxysmal nocturnal hemoglobinuria
- Myelodysplastic syndrome
- Hemoglobinopathy
- Von Willebrand disease
- Diamond-Blackfan anemia
- Chronic myelomonocytic leukemia
- 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
Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm Universitätsklinikum Ulm
Eythstrasse 24
89075 Ulm
- Quantitative and/or qualitative congenital phagocyte defect
- Paroxysmal nocturnal hemoglobinuria
- Severe combined immunodeficiency
- Alpha-thalassemia
- Rare anemia
- Hereditary spherocytosis
- Sickle cell anemia
- Beta-thalassemia
- Primary immunodeficiency due to a defect in innate immunity
- Immunodeficiency predominantly affecting antibody production
- Polycythemia
- Autoimmune thrombocytopenia
- Autoinflammatory syndrome of childhood
- Immune dysregulation disease with immunodeficiency
- Syndrome with combined immunodeficiency
Zentrum für angeborene Blutzellerkrankungen am Universitätsklinikum Würzburg
Universitätsklinikum Würzburg Zentrum für Seltene Erkrankungen - Referenzzentrum Nordbayern (ZESE)
Josef-Schneider-Straße 2
97080 Würzburg
- Hemolytic anemia due to red cell pyruvate kinase deficiency
- Congenital dyserythropoietic anemia
- Fanconi anemia
- Class I glucose-6-phosphate dehydrogenase deficiency
- Hemoglobinopathy
- Bernard-Soulier syndrome
- Beta-thalassemia and related diseases
- Sickle cell anemia
- Hermansky-Pudlak syndrome
- Glanzmann thrombasthenia
- Alpha-thalassemia and related disorders
- Hereditary stomatocytosis
- MYH9-related disease
- Hereditary spherocytosis
- Alpha-thalassemia