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