Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
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Klinik und Poliklinik für Pädiatrische Hämatologie und Onkologie am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE) Martin Zeitz Centrum für Seltene Erkrankungen (MZCSE)
Martinistraße 52
20251 Hamburg
040 741054270
040 741054601
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- Rhabdomyosarcoma
- Congenital factor V deficiency
- Retinoblastoma
- Hemophilia
- Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome
- Alveolar soft tissue sarcoma
- Medulloblastoma
- Sickle cell anemia
- Beta-thalassemia
- Combined T and B cell immunodeficiency
- Fanconi anemia
- Alpha-thalassemia
- Von Willebrand disease
Zentrum für seltene Stoffwechselerkrankungen der Medizinischen Hochschule Hannover
Zentrum für Seltene Erkrankungen Hannover Medizinische Hochschule Hannover
Carl-Neuberg-Straße 1
30625 Hannover
Zentrum für Seltene Störungen der Hämatopoese und Immundefekte (ZSHI) am Universitätsklinikum Ulm
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstrasse 24
89075 Ulm
- Hereditary spherocytosis
- Rare anemia
- Quantitative and/or qualitative congenital phagocyte defect
- Paroxysmal nocturnal hemoglobinuria
- Severe combined immunodeficiency
- Alpha-thalassemia
- Autoinflammatory syndrome of childhood
- Immunodeficiency predominantly affecting antibody production
- Primary immunodeficiency due to a defect in innate immunity
- Polycythemia
- Beta-thalassemia
- Sickle cell anemia
- Autoimmune thrombocytopenia
- Syndrome with combined immunodeficiency
- Immune dysregulation disease with immunodeficiency
Zentrum für angeborene Blutzellerkrankungen am Universitätsklinikum Würzburg
Zentrum für Seltene Erkrankungen - Referenzzentrum Nordbayern (ZESE) Universitätsklinikum Würzburg
Josef-Schneider-Straße 2
97080 Würzburg
- Congenital dyserythropoietic anemia
- Hereditary stomatocytosis
- Alpha-thalassemia
- Fanconi anemia
- Sickle cell anemia
- Hemoglobinopathy
- Class I glucose-6-phosphate dehydrogenase deficiency
- Beta-thalassemia and related diseases
- MYH9-related disease
- Hemolytic anemia due to red cell pyruvate kinase deficiency
- Glanzmann thrombasthenia
- Alpha-thalassemia and related disorders
- Bernard-Soulier syndrome
- Hermansky-Pudlak syndrome
- Hereditary spherocytosis