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
- Li-Fraumeni syndrome
- Xeroderma pigmentosum
- Hereditary retinoblastoma
- Ataxia-telangiectasia
- Common variable immunodeficiency
- Silver-Russell syndrome
- Hereditary nonpolyposis colon cancer
- Familial ovarian cancer
- Von Hippel-Lindau disease
- Inherited cancer-predisposing syndrome
- Diamond-Blackfan anemia
- Full NF2-related schwannomatosis
- Constitutional mismatch repair deficiency syndrome
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Website
Email
- Costello syndrome
- Ataxia-telangiectasia
- Silver-Russell syndrome
- Von Hippel-Lindau disease
- Maffucci syndrome
- Noonan syndrome
- Li-Fraumeni syndrome
- Beckwith-Wiedemann syndrome
- Xeroderma pigmentosum
- Cockayne syndrome
- Familial ovarian cancer
- Diamond-Blackfan anemia
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Inherited renal cancer-predisposing 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
- Congenital factor V deficiency
- Retinoblastoma
- Rhabdomyosarcoma
- Alveolar soft tissue sarcoma
- Alpha-thalassemia
- Hemophilia
- Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome
- Medulloblastoma
- Sickle cell anemia
- Fanconi anemia
- Combined T and B cell immunodeficiency
- Von Willebrand disease
- Beta-thalassemia