Ollier disease
Parent facilities 0
Genetic Advices 2
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
Website
Email
- Ataxia-telangiectasia
- Full NF2-related schwannomatosis
- Silver-Russell syndrome
- Hereditary nonpolyposis colon cancer
- Hereditary retinoblastoma
- Von Hippel-Lindau disease
- Constitutional mismatch repair deficiency syndrome
- Li-Fraumeni syndrome
- Noonan syndrome
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Inherited cancer-predisposing syndrome
- Diamond-Blackfan anemia
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Website
Email
- Silver-Russell syndrome
- Diamond-Blackfan anemia
- Von Hippel-Lindau disease
- Inherited renal cancer-predisposing syndrome
- Li-Fraumeni syndrome
- Full NF2-related schwannomatosis
- Xeroderma pigmentosum
- Beckwith-Wiedemann syndrome
- Cockayne syndrome
- Noonan syndrome
- Ataxia-telangiectasia
- Costello syndrome
- Maffucci syndrome
Care facilities 5
Zentrum für Gesichts- und Skelettfehlbildungen der Uniklinik RWTH Aachen
Uniklinik RWTH Aachen Zentrum für Seltene Erkrankungen Aachen
Pauwelsstraße 30
52074 Aachen
0241 88807150
0241 803387021
Website
Email
Klinik für Hämatologie, Onkologie und Palliativmedizin am HELIOS Klinikum Bad Saarow
HELIOS Klinikum Bad Saarow
Pieskower Straße 33
15526 Bad Saarow
Zentrum für angeborene Stoffwechselerkrankungen am Universitätsklinikum Freiburg
Universitätsklinikum Freiburg Freiburg Zentrum für Seltene Erkrankungen (FZSE)
Breisacherstr. 62
79106 Freiburg
- Glucose-galactose malabsorption
- Glycogen storage disease
- Maple syrup urine disease
- Gluconeogenesis disorder
- Hereditary fructose intolerance
- Disorder of fatty acid oxidation and ketone body metabolism
- Disorder of fructose metabolism
- Fabry disease
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
- Disorder of branched-chain amino acid metabolism
- Disorder of ketolysis
- Disorder of galactose metabolism
Altonaer Kinderkrankenhaus
Bleickenallee 38
22763 Hamburg
040 889080
040 88908366
Website
Email
- Neural tube defect
- Autosomal dominant polycystic kidney disease
- 22q11.2 deletion syndrome
- Neurocutaneous melanocytosis
- Large congenital melanocytic nevus
- Autosomal recessive polycystic kidney disease
- Diaphragmatic or abdominal wall malformation
- Osteogenesis imperfecta
- Rare bone disease
- Digestive tract malformation
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Centrum für Seltene Erkrankungen Köln (CESEK) Uniklinik Köln
Kerpener Straße 62
50937 Köln
- Brachydactyly-long thumb syndrome
- Femur-fibula-ulna complex
- Rhizomelic chondrodysplasia punctata type 1
- Multiple osteochondromas
- Dysosteosclerosis
- Hypochondroplasia
- Osteogenesis imperfecta
- Fibrous dysplasia of bone
- Achondroplasia
- Heart-hand syndrome
- Omodysplasia
- Acromelic dysplasia
- Metachondromatosis
- Paralytic facial malformation