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
- Noonan syndrome
- Beckwith-Wiedemann syndrome
- Constitutional mismatch repair deficiency syndrome
- Xeroderma pigmentosum
- Common variable immunodeficiency
- Hereditary retinoblastoma
- Hereditary nonpolyposis colon cancer
- Silver-Russell syndrome
- Ataxia-telangiectasia
- Von Hippel-Lindau disease
- Diamond-Blackfan anemia
- Familial ovarian cancer
- Inherited cancer-predisposing syndrome
- Full NF2-related schwannomatosis
- Li-Fraumeni syndrome
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Website
Email
- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Familial ovarian cancer
- Costello syndrome
- Xeroderma pigmentosum
- Silver-Russell syndrome
- Maffucci syndrome
- Beckwith-Wiedemann syndrome
- Cockayne syndrome
- Ataxia-telangiectasia
- Diamond-Blackfan anemia
- Inherited renal cancer-predisposing syndrome
- Li-Fraumeni syndrome
- Noonan syndrome
Care facilities 2
Zentrum für Gefäßfehlbildungen am Universitätsklinikum Freiburg
Freiburg Zentrum für Seltene Erkrankungen (FZSE) Universitätsklinikum Freiburg
Breisacher Str. 62
79106 Freiburg
0761 27043021
0761 2709643366
Website
Email
Klinik und Poliklinik für Pädiatrische Hämatologie und Onkologie am Universitätsklinikum Hamburg-Eppendorf
Martin Zeitz Centrum für Seltene Erkrankungen (MZCSE) Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741054270
040 741054601
Website
Email
- Retinoblastoma
- Rhabdomyosarcoma
- Alveolar soft tissue sarcoma
- Medulloblastoma
- Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome
- Hemophilia
- Alpha-thalassemia
- Combined T and B cell immunodeficiency
- Congenital factor V deficiency
- Von Willebrand disease
- Beta-thalassemia
- Fanconi anemia
- Sickle cell anemia