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