Syndromes with skeletal anomalies as a major feature
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
code elsewhere
- Progressive osseous heteroplasia (FB31.0)
- Fibrodysplasia ossificans progressiva (FB31.1)
- Osteolysis syndromes (FB86.2)
- Calcification or ossification of muscles of genetic origin (FB31.Z)
sections/codes in this section (LD24-LD24)
- Syndromes with micromelia (LD24.0)
- Bone diseases with increased bone density (LD24.1)
- Bone diseases with disorganised development of skeletal components (LD24.2)
- Spondyloepiphyseal or spondyloepimetaphyseal dysplasias (LD24.3)
- Spondylometaphyseal dysplasias (LD24.4)
- Spondylodysplastic dysplasias (LD24.5)
- Multiple epiphyseal dysplasia or pseudoachondroplasia (LD24.6)
- Multiple metaphyseal dysplasias (LD24.7)
- Acromelic dysplasias (LD24.8)
- Acromesomelic dysplasias (LD24.9)
- Mesomelic or rhizomesomelic dysplasias (LD24.A)
- Short rib syndromes (LD24.B)
- Bent bone dysplasias (LD24.C)
- Slender bone dysplasias (LD24.D)
- Bone dysplasias with multiple joint dislocations (LD24.E)
- Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments (LD24.F)
- Syndromic craniosynostoses (LD24.G)
- Dysostoses with predominant vertebral and costal involvement (LD24.H)
- Patellar dysostoses (LD24.J)
- Genetic bone diseases with decreased bone density (LD24.K)
- Other specified syndromes with skeletal anomalies as a major feature (LD24.Y)
- Syndromes with skeletal anomalies as a major feature, unspecified (LD24.Z)
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