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