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