Angioosteohypotrophic syndrome
Parent facilities 0
Genetic Advices 1
Institut für Medizinische Genetik und Humangenetik an der Charité Berlin
Charité Universitätsmedizin Berlin Berliner Centrum für Seltene Erkrankungen (BCSE)
Augustenburger Platz 1
13353 Berlin
030 450569122
030 450569915
Website
Care facilities 2
Altonaer Kinderkrankenhaus
Bleickenallee 38
22763 Hamburg
040 889080
040 88908366
Website
Email
- Autosomal dominant polycystic kidney disease
- 22q11.2 deletion syndrome
- Neurocutaneous melanocytosis
- Neural tube defect
- Diaphragmatic or abdominal wall malformation
- Osteogenesis imperfecta
- Digestive tract malformation
- Large congenital melanocytic nevus
- Autosomal recessive polycystic kidney disease
- Rare bone disease
Zentrum für seltene kranio-orofaziale Erkrankungen am Universitätsklinikum Heidelberg
Centre for Rare Diseases Heidelberg Universitätsklinikum Heidelberg
Im Neuenheimer Feld 400
69120 Heidelberg
- Paramedian facial cleft
- Median facial cleft
- Noonan syndrome
- Facial cleft
- Isolated Pierre Robin syndrome
- Apert syndrome
- Papillon-Lefèvre syndrome
- GAPO syndrome
- Orofaciodigital syndrome type 2
- Seckel syndrome
- Non-syndromic metopic craniosynostosis
- Oblique facial cleft
- Van der Woude syndrome
- Crouzon syndrome
- Saethre-Chotzen syndrome