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
- Xeroderma pigmentosum
- Familial ovarian cancer
- Hereditary retinoblastoma
- Li-Fraumeni syndrome
- Beckwith-Wiedemann syndrome
- Von Hippel-Lindau disease
- Inherited cancer-predisposing syndrome
- Constitutional mismatch repair deficiency syndrome
- Noonan syndrome
- Silver-Russell syndrome
- Diamond-Blackfan anemia
- Hereditary nonpolyposis colon cancer
- Full NF2-related schwannomatosis
- Ataxia-telangiectasia
- Common variable immunodeficiency
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Website
Email
- Silver-Russell syndrome
- Ataxia-telangiectasia
- Von Hippel-Lindau disease
- Costello syndrome
- Maffucci syndrome
- Beckwith-Wiedemann syndrome
- Noonan syndrome
- Cockayne syndrome
- Xeroderma pigmentosum
- Diamond-Blackfan anemia
- Familial ovarian cancer
- Inherited renal cancer-predisposing syndrome
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Li-Fraumeni 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
Frankfurter Referenzzentrum für Seltene Erkrankungen (FRZSE) Universitätsmedizin Frankfurt
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
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstrasse 24
89075 Ulm
- Immune dysregulation disease with immunodeficiency
- Autoinflammatory syndrome of childhood
- Quantitative and/or qualitative congenital phagocyte defect
- Sickle cell anemia
- Syndrome with combined immunodeficiency
- Autoimmune thrombocytopenia
- Beta-thalassemia
- Polycythemia
- Immunodeficiency predominantly affecting antibody production
- Rare anemia
- Primary immunodeficiency due to a defect in innate immunity
- Severe combined immunodeficiency
- Paroxysmal nocturnal hemoglobinuria
- Alpha-thalassemia
- Hereditary spherocytosis