Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome
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
- Noonan syndrome
- Common variable immunodeficiency
- Silver-Russell syndrome
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
- Hereditary retinoblastoma
- Ataxia-telangiectasia
- Von Hippel-Lindau disease
- Constitutional mismatch repair deficiency syndrome
- Li-Fraumeni syndrome
- Inherited cancer-predisposing 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
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Li-Fraumeni syndrome
- Noonan syndrome
- Maffucci syndrome
- Inherited renal cancer-predisposing syndrome
- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Diamond-Blackfan anemia
- Familial ovarian cancer
- Ataxia-telangiectasia
- Costello syndrome
- Silver-Russell syndrome
- Cockayne syndrome
Care facilities 2
Zentrum für Gefäßfehlbildungen am Universitätsklinikum Freiburg
Universitätsklinikum Freiburg Freiburg Zentrum für Seltene Erkrankungen (FZSE)
Breisacher Str. 62
79106 Freiburg
0761 27043021
0761 2709643366
Website
Email
Klinik und Poliklinik für Pädiatrische Hämatologie und Onkologie am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE) Martin Zeitz Centrum für Seltene Erkrankungen (MZCSE)
Martinistraße 52
20251 Hamburg
040 741054270
040 741054601
Website
Email
- Rhabdomyosarcoma
- Hemophilia
- Congenital factor V deficiency
- Retinoblastoma
- Alveolar soft tissue sarcoma
- Medulloblastoma
- Alpha-thalassemia
- Von Willebrand disease
- Fanconi anemia
- Combined T and B cell immunodeficiency
- Beta-thalassemia
- Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome
- Sickle cell anemia