Inherited cancer-predisposing syndrome
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Genetic Advices 3
Zentrum für Klinische Genommedizin am Universitätsklinikum Dresden
UniversitätsCentrum für Seltene Erkrankungen Dresden (USE) Universitätsklinikum Carl Gustav Carus Dresden
Fetscherstraße 74
01307 Dresden
0351 4585136
0351 4586337
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- Inherited cancer-predisposing syndrome
- Rare pervasive developmental disorder
- Familial pancreatic carcinoma
- Rare intellectual disability
- Hereditary gastric cancer
- Familial adenomatous polyposis
- Hereditary breast cancer
- Li-Fraumeni syndrome
- Hereditary nonpolyposis colon cancer
- Multiple endocrine neoplasia
- Ovarian cancer
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
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- Noonan syndrome
- Beckwith-Wiedemann syndrome
- Diamond-Blackfan anemia
- Li-Fraumeni syndrome
- Constitutional mismatch repair deficiency syndrome
- Familial ovarian cancer
- Von Hippel-Lindau disease
- Inherited cancer-predisposing syndrome
- Full NF2-related schwannomatosis
- Hereditary retinoblastoma
- Hereditary nonpolyposis colon cancer
- Xeroderma pigmentosum
- Common variable immunodeficiency
- Silver-Russell syndrome
- 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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- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Von Hippel-Lindau disease
- Ataxia-telangiectasia
- Silver-Russell syndrome
- Maffucci syndrome
- Xeroderma pigmentosum
- Cockayne syndrome
- Costello syndrome
- Beckwith-Wiedemann syndrome
- Diamond-Blackfan anemia
- Inherited renal cancer-predisposing syndrome
- Noonan syndrome
- Li-Fraumeni syndrome
- Familial ovarian cancer
Care facilities 4
Zentrum für seltene Lebererkrankungen und gastrointestinale Erkrankungen der Uniklinik RWTH Aachen
Uniklinik RWTH Aachen Zentrum für Seltene Erkrankungen Aachen
Pauwelsstr. 30
52074 Aachen
- Primary sclerosing cholangitis
- Cholangiocarcinoma
- Alpha-1-antitrypsin deficiency
- Porphyria
- Peutz-Jeghers syndrome
- HJV or HAMP-related hemochromatosis
- Congenital erythropoietic porphyria
- TFR2-related hemochromatosis
- VIPoma
- Familial adenomatous polyposis
- Wilson disease
- Budd-Chiari syndrome
- Hereditary chronic pancreatitis
- Primary biliary cholangitis
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
- Essential thrombocythemia
- Aggressive systemic mastocytosis
- Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
- Mast cell leukemia
- Chronic myeloid leukemia
- Autosomal dominant aplasia and myelodysplasia
- Dyskeratosis congenita
- Idiopathic aplastic anemia
- Myelodysplastic syndrome
- Classic mast cell leukemia
- Paroxysmal nocturnal hemoglobinuria
Zentrum für Tumordispositionssyndrome (ZeKiTDS) - Kinder und Erwachsene 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