Other specified syndromes with skeletal anomalies as a major feature

Exclusions from above levels

LD24.0 – Syndromes with micromelia
LD24.1 – Bone diseases with increased bone density
LD24.2 – Bone diseases with disorganised development of skeletal components
LD24.3 – Spondyloepiphyseal or spondyloepimetaphyseal dysplasias
LD24.4 – Spondylometaphyseal dysplasias
LD24.5 – Spondylodysplastic dysplasias
LD24.6 – Multiple epiphyseal dysplasia or pseudoachondroplasia
LD24.7 – Multiple metaphyseal dysplasias
LD24.8 – Acromelic dysplasias
LD24.9 – Acromesomelic dysplasias
LD24.A – Mesomelic or rhizomesomelic dysplasias
LD24.B – Short rib syndromes
LD24.C – Bent bone dysplasias
LD24.D – Slender bone dysplasias
LD24.E – Bone dysplasias with multiple joint dislocations
LD24.F – Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments
LD24.G – Syndromic craniosynostoses
LD24.H – Dysostoses with predominant vertebral and costal involvement
LD24.J – Patellar dysostoses
LD24.K – Genetic bone diseases with decreased bone density
LD24.Z – Syndromes with skeletal anomalies as a major feature, unspecified

Part of: LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies