BAP1-related tumor predisposition syndrome
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Genetic Advices 2
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
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- Ataxia-telangiectasia
- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- Hereditary retinoblastoma
- Familial ovarian cancer
- Constitutional mismatch repair deficiency syndrome
- Common variable immunodeficiency
- Xeroderma pigmentosum
- Li-Fraumeni syndrome
- Inherited cancer-predisposing syndrome
- Diamond-Blackfan anemia
- Silver-Russell syndrome
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
- Noonan syndrome
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
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- Li-Fraumeni syndrome
- Maffucci syndrome
- Inherited renal cancer-predisposing syndrome
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Diamond-Blackfan anemia
- Familial ovarian cancer
- Von Hippel-Lindau disease
- Noonan syndrome
- Silver-Russell syndrome
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Costello syndrome
- Cockayne syndrome
- Ataxia-telangiectasia
Care facilities 1
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
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- Von Willebrand disease
- Beta-thalassemia
- Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome
- Fanconi anemia
- Alpha-thalassemia
- Combined T and B cell immunodeficiency
- Sickle cell anemia
- Alveolar soft tissue sarcoma
- Medulloblastoma
- Rhabdomyosarcoma
- Congenital factor V deficiency
- Retinoblastoma
- Hemophilia