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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- Noonan syndrome
- Beckwith-Wiedemann syndrome
- Inherited cancer-predisposing syndrome
- Xeroderma pigmentosum
- Familial ovarian cancer
- Diamond-Blackfan anemia
- Li-Fraumeni syndrome
- Full NF2-related schwannomatosis
- Hereditary nonpolyposis colon cancer
- Von Hippel-Lindau disease
- Common variable immunodeficiency
- Silver-Russell syndrome
- Ataxia-telangiectasia
- Constitutional mismatch repair deficiency 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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- Familial ovarian cancer
- Cockayne syndrome
- Beckwith-Wiedemann syndrome
- Li-Fraumeni syndrome
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Maffucci syndrome
- Costello syndrome
- Inherited renal cancer-predisposing syndrome
- Xeroderma pigmentosum
- Ataxia-telangiectasia
- Silver-Russell syndrome
- Diamond-Blackfan anemia
- Von Hippel-Lindau disease
- 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
- Hereditary isolated aplastic anemia
- Mastocytosis
- Chronic eosinophilic leukemia
- Chronic myeloproliferative disease, unclassifiable
- Dyskeratosis congenita
- Idiopathic aplastic anemia
- Myelodysplastic syndrome
- Classic mast cell leukemia
- Paroxysmal nocturnal hemoglobinuria
- Chronic myeloid leukemia
- Mast cell leukemia
- Autosomal dominant aplasia and myelodysplasia
- Essential thrombocythemia
- Aggressive systemic mastocytosis
- Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Zentrum für seltene Lebererkrankungen und gastrointestinale Erkrankungen der Uniklinik RWTH Aachen
Uniklinik RWTH Aachen Zentrum für Seltene Erkrankungen Aachen
Pauwelsstr. 30
52074 Aachen
- Alpha-1-antitrypsin deficiency
- Primary sclerosing cholangitis
- Congenital erythropoietic porphyria
- Peutz-Jeghers syndrome
- HJV or HAMP-related hemochromatosis
- Porphyria
- TFR2-related hemochromatosis
- Hereditary chronic pancreatitis
- VIPoma
- Fabry disease
- Primary biliary cholangitis
- Wilson disease
- Budd-Chiari syndrome
- Cholangiocarcinoma
- Familial adenomatous polyposis
Zentrum für Tumordispositionssyndrome (ZeKiTDS) 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
Essener Zentrum für Seltene Erkrankungen (EZSE) Universitätsklinikum Essen
Hufelandstr. 55
45147 Essen