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