Tarsal-carpal coalition syndrome
All Entries 2
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Uniklinik Köln Centrum für Seltene Erkrankungen Köln (CESEK)
                    Kerpener Straße 62
                    50937 Köln 
                
- Rhizomelic chondrodysplasia punctata type 1
- Omodysplasia
- OBSOLETE: Peripheral dysostosis
- Brachydactyly-long thumb syndrome
- Metachondromatosis
- Fibrous dysplasia of bone
- Dysosteosclerosis
- Osteogenesis imperfecta
- Paralytic facial malformation
- Hypochondroplasia
- Multiple osteochondromas
- Femur-fibula-ulna complex
- Heart-hand syndrome
- Acromelic dysplasia
- Achondroplasia
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Achondroplasia
- Isolated growth hormone deficiency type III
- Hypochondroplasia
- Laron syndrome
- FGFR3-related chondrodysplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Diastrophic dysplasia
- Silver-Russell syndrome
- Thanatophoric dysplasia
- Seckel syndrome
- Spondyloepiphyseal dysplasia congenita
- Pseudoachondroplasia
- Non-acquired isolated growth hormone deficiency
Parent facilities 0
Genetic Advices 0
Care facilities 1
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Uniklinik Köln Centrum für Seltene Erkrankungen Köln (CESEK)
                    Kerpener Straße 62
                    50937 Köln 
                
- Rhizomelic chondrodysplasia punctata type 1
- Omodysplasia
- OBSOLETE: Peripheral dysostosis
- Brachydactyly-long thumb syndrome
- Metachondromatosis
- Fibrous dysplasia of bone
- Dysosteosclerosis
- Osteogenesis imperfecta
- Paralytic facial malformation
- Hypochondroplasia
- Multiple osteochondromas
- Femur-fibula-ulna complex
- Heart-hand syndrome
- Acromelic dysplasia
- Achondroplasia
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Achondroplasia
- Isolated growth hormone deficiency type III
- Hypochondroplasia
- Laron syndrome
- FGFR3-related chondrodysplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Diastrophic dysplasia
- Silver-Russell syndrome
- Thanatophoric dysplasia
- Seckel syndrome
- Spondyloepiphyseal dysplasia congenita
- Pseudoachondroplasia
- Non-acquired isolated growth hormone deficiency