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