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 venous malformation
- Rare hemolytic anemia
- Chronic myelomonocytic leukemia
- Von Willebrand disease
- Beta-thalassemia
- Juvenile myelomonocytic leukemia
- Rare capillary malformation
- Hemoglobinopathy
- Rare aplastic anemia
- Congenital factor XI deficiency
- Rare lymphatic malformation
- Myelodysplastic syndrome
- Diamond-Blackfan anemia
- Paroxysmal nocturnal hemoglobinuria
Klinik für Kinder und Jugendmedizin- Pädiatrische Hämatologie & Onkologie am Universitätsklinikum Münster
Centrum für seltene Erkrankungen Münster Universitätsklinikum Münster (UKM)
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
- Immune dysregulation disease with immunodeficiency
- Quantitative and/or qualitative congenital phagocyte defect
- Rare anemia
- Paroxysmal nocturnal hemoglobinuria
- Hereditary spherocytosis
- Alpha-thalassemia
- Severe combined immunodeficiency
- Polycythemia
- Primary immunodeficiency due to a defect in innate immunity
- Beta-thalassemia
- Immunodeficiency predominantly affecting antibody production
- Autoinflammatory syndrome of childhood
- Autoimmune thrombocytopenia
- Syndrome with combined immunodeficiency
- 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
- Bernard-Soulier syndrome
- Hermansky-Pudlak syndrome
- Hemolytic anemia due to red cell pyruvate kinase deficiency
- Alpha-thalassemia and related disorders
- Beta-thalassemia and related diseases
- Glanzmann thrombasthenia
- Hereditary stomatocytosis
- Fanconi anemia
- MYH9-related disease
- Sickle cell anemia
- Hemoglobinopathy
- Class I glucose-6-phosphate dehydrogenase deficiency
- Congenital dyserythropoietic anemia
- Hereditary spherocytosis
- Alpha-thalassemia