Inherited cancer-predisposing 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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- Inherited cancer-predisposing syndrome
- Diamond-Blackfan anemia
- Silver-Russell syndrome
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
- Noonan syndrome
- Hereditary retinoblastoma
- Ataxia-telangiectasia
- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- Familial ovarian cancer
- Constitutional mismatch repair deficiency syndrome
- Common variable immunodeficiency
- Xeroderma pigmentosum
- Li-Fraumeni syndrome
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
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- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- Ataxia-telangiectasia
- Li-Fraumeni syndrome
- APC-related attenuated familial adenomatous polyposis
- Familial ovarian cancer
- Diamond-Blackfan anemia
- Inherited renal cancer-predisposing syndrome
- Noonan syndrome
- Xeroderma pigmentosum
- Silver-Russell syndrome
- Maffucci syndrome
- Cockayne syndrome
- Costello syndrome
- Beckwith-Wiedemann syndrome
Care facilities 4
Zentrum für seltene hämatologische Erkrankungen der Uniklinik RWTH Aachen
Zentrum für Seltene Erkrankungen Aachen Uniklinik RWTH Aachen
Pauwelsstr. 30
52074 Aachen
- Chronic myeloproliferative disease, unclassifiable
- Dyskeratosis congenita
- Essential thrombocythemia
- Hereditary isolated aplastic anemia
- Idiopathic aplastic anemia
- Autosomal dominant aplasia and myelodysplasia
- Chronic eosinophilic leukemia
- Mastocytosis
- Classic mast cell leukemia
- Mast cell leukemia
- Paroxysmal nocturnal hemoglobinuria
- Myelodysplastic syndrome
- Chronic myeloid leukemia
- Aggressive systemic mastocytosis
- Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Zentrum für seltene Lebererkrankungen und gastrointestinale Erkrankungen der Uniklinik RWTH Aachen
Zentrum für Seltene Erkrankungen Aachen Uniklinik RWTH Aachen
Pauwelsstr. 30
52074 Aachen
- Peutz-Jeghers syndrome
- Familial adenomatous polyposis
- Congenital erythropoietic porphyria
- Cholangiocarcinoma
- Primary sclerosing cholangitis
- VIPoma
- Hereditary chronic pancreatitis
- Budd-Chiari syndrome
- Alpha-1-antitrypsin deficiency
- TFR2-related hemochromatosis
- HJV or HAMP-related hemochromatosis
- Primary biliary cholangitis
- Fabry disease
- Wilson disease
- Porphyria
Interdisziplinäres Zentrum für Kinder, Jugendliche und Erwachsene mit Tumordispositionssyndromen am Universitätsklinikum Augsburg
Augsburger Zentrum für Seltene Erkrankungen (AZeSE)
Stenglinstraße 2
86156 Augsburg
0821 4009300
0821 400179330
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Zentrum für Menschen mit Hämoglobinopathien am Universitätsklinikum Essen
Universitätsklinikum Essen Essener Zentrum für Seltene Erkrankungen (EZSE)
Hufelandstr. 55
45147 Essen