Catalog
Syndromes with skeletal anomalies as a major feature
Link to WHO Definition
Syndromes with skeletal anomalies as a major feature – http://id.who.int/icd/entity/1496140949
Parents
Children
- LD24.K Genetic bone diseases with decreased bone density
- LD24.J Patellar dysostoses
- LD24.0 Syndromes with micromelia
- LD24.8 Acromelic dysplasias
- LD24.4 Spondylometaphyseal dysplasias
- LD24.G Syndromic craniosynostoses
- LD24.2 Bone diseases with disorganised development of skeletal components
- LD24.3 Spondyloepiphyseal or spondyloepimetaphyseal dysplasias
- LD24.9 Acromesomelic dysplasias
- LD24.6 Multiple epiphyseal dysplasia or pseudoachondroplasia
- LD24.1 Bone diseases with increased bone density
- LD24.F Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments
- LD24.5 Spondylodysplastic dysplasias
- LD24.H Dysostoses with predominant vertebral and costal involvement
- LD24.B Short rib syndromes
- LD24.A Mesomelic or rhizomesomelic dysplasias
- Calcification or ossification of muscles of genetic origin
- Osteolysis syndromes
- LD24.E Bone dysplasias with multiple joint dislocations
- LD24.D Slender bone dysplasias
- LD24.7 Multiple metaphyseal dysplasias
- LD24.C Bent bone dysplasias