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
- Constitutional mismatch repair deficiency syndrome
- Hereditary retinoblastoma
- Familial ovarian cancer
- Von Hippel-Lindau disease
- Xeroderma pigmentosum
- Common variable immunodeficiency
- Ataxia-telangiectasia
- Full NF2-related schwannomatosis
- Diamond-Blackfan anemia
- Li-Fraumeni syndrome
- Hereditary nonpolyposis colon cancer
- Inherited cancer-predisposing syndrome
- Silver-Russell syndrome
- Noonan syndrome
- Beckwith-Wiedemann 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
- Li-Fraumeni syndrome
- Maffucci syndrome
- Noonan syndrome
- Inherited renal cancer-predisposing syndrome
- Beckwith-Wiedemann syndrome
- Xeroderma pigmentosum
- Silver-Russell syndrome
- Cockayne syndrome
- APC-related attenuated familial adenomatous polyposis
- Ataxia-telangiectasia
- Full NF2-related schwannomatosis
- Costello syndrome
- Familial ovarian cancer
- Von Hippel-Lindau disease
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
- Primary immunodeficiency due to a defect in innate immunity
- Autoinflammatory syndrome of childhood
- Polycythemia
- Immunodeficiency predominantly affecting antibody production
- Autoimmune thrombocytopenia
- Beta-thalassemia
- Immune dysregulation disease with immunodeficiency
- Sickle cell anemia
- Syndrome with combined immunodeficiency
- Hereditary spherocytosis
- Quantitative and/or qualitative congenital phagocyte defect
- Rare anemia
- Paroxysmal nocturnal hemoglobinuria
- Alpha-thalassemia
- Severe combined immunodeficiency