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