Combined immunodeficiency due to OX40 deficiency
Parent facilities 0
Genetic Advices 2
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
Website
Email
- Noonan syndrome
- Silver-Russell syndrome
- Xeroderma pigmentosum
- Common variable immunodeficiency
- Hereditary retinoblastoma
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
- Full NF2-related schwannomatosis
- Ataxia-telangiectasia
- Von Hippel-Lindau disease
- Constitutional mismatch repair deficiency syndrome
- Li-Fraumeni syndrome
- Diamond-Blackfan anemia
- Familial ovarian cancer
- Inherited cancer-predisposing syndrome
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Website
Email
- Diamond-Blackfan anemia
- Silver-Russell syndrome
- Maffucci syndrome
- Noonan syndrome
- Beckwith-Wiedemann syndrome
- Costello syndrome
- Familial ovarian cancer
- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Ataxia-telangiectasia
- Cockayne syndrome
- Li-Fraumeni syndrome
- Xeroderma pigmentosum
- Inherited renal cancer-predisposing syndrome
Care facilities 3
Zentrum für angeborene Störungen des Immunsystems (ZASI) am Universitätsklinikum Düsseldorf
Zentrum für Seltene Erkrankungen Düsseldorf (ZSED)
Moorenstraße 5
40225 Düsseldorf
Zentrum für Pädiatrische Stammzelltransplantation und Immunologie der Universitätsmedizin Frankfurt
Universitätsmedizin Frankfurt Frankfurter Referenzzentrum für Seltene Erkrankungen (FRZSE)
Theodor-Stern-Kai 7
60590 Frankfurt am Main
069 63016063
069 63014202
Website
069 63016063
069 63014202
Website
Zentrum für Seltene Störungen der Hämatopoese und Immundefekte (ZSHI) am Universitätsklinikum Ulm
Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm Universitätsklinikum Ulm
Eythstrasse 24
89075 Ulm
- Sickle cell anemia
- Immunodeficiency predominantly affecting antibody production
- Beta-thalassemia
- Polycythemia
- Primary immunodeficiency due to a defect in innate immunity
- Severe combined immunodeficiency
- Alpha-thalassemia
- Rare anemia
- Immune dysregulation disease with immunodeficiency
- Hereditary spherocytosis
- Paroxysmal nocturnal hemoglobinuria
- Autoinflammatory syndrome of childhood
- Syndrome with combined immunodeficiency
- Autoimmune thrombocytopenia
- Quantitative and/or qualitative congenital phagocyte defect