Isolated hemihyperplasia
All Entries 4
Zentrum für Gefäßfehlbildungen am Universitätsklinikum Freiburg
Freiburg Zentrum für Seltene Erkrankungen (FZSE) Universitätsklinikum Freiburg
Breisacher Str. 62
79106 Freiburg
0761 27043021
0761 2709643366
Website
Email
- Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome
- Vein of Galen aneurysmal malformation
- Dural sinus malformation
- Facial arteriovenous malformation
- Beckwith-Wiedemann syndrome
- Primary lymphedema
- Von Hippel-Lindau disease
- Macrocystic lymphatic malformation
- Rare venous malformation
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
Website
Email
- Ataxia-telangiectasia
- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- Hereditary retinoblastoma
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
- Xeroderma pigmentosum
- Common variable immunodeficiency
- Silver-Russell syndrome
- Inherited cancer-predisposing syndrome
- Diamond-Blackfan anemia
- Li-Fraumeni syndrome
- Noonan syndrome
- Constitutional mismatch repair deficiency syndrome
- Familial ovarian cancer
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Website
Email
- 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
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
- Von Hippel-Lindau disease
- Full NF2-related schwannomatosis
- Hereditary retinoblastoma
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
- Xeroderma pigmentosum
- Common variable immunodeficiency
- Silver-Russell syndrome
- Inherited cancer-predisposing syndrome
- Diamond-Blackfan anemia
- Li-Fraumeni syndrome
- Noonan syndrome
- Constitutional mismatch repair deficiency syndrome
- Familial ovarian cancer
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
Website
Email
- 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 1
Zentrum für Gefäßfehlbildungen am Universitätsklinikum Freiburg
Freiburg Zentrum für Seltene Erkrankungen (FZSE) Universitätsklinikum Freiburg
Breisacher Str. 62
79106 Freiburg
0761 27043021
0761 2709643366
Website
Email
- Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome
- Vein of Galen aneurysmal malformation
- Dural sinus malformation
- Facial arteriovenous malformation
- Beckwith-Wiedemann syndrome
- Primary lymphedema
- Von Hippel-Lindau disease
- Macrocystic lymphatic malformation
- Rare venous malformation