Syndromes with skeletal anomalies as a major feature

Child codes

• 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.Y – Other specified syndromes with skeletal anomalies as a major feature
• LD24.Z – Syndromes with skeletal anomalies as a major feature, unspecified

Foundation children elsewhere

• FB31.0 – Progressive osseous heteroplasia
• FB31.1 – Fibrodysplasia ossificans progressiva

Sibling codes

• LD20 – Syndromes with central nervous system anomalies as a major feature
• LD21 – Syndromes with eye anomalies as a major feature
• LD22 – Syndromes with dental anomalies as a major feature
• LD23 – Syndromes with vascular anomalies as a major feature
• LD25 – Syndromes with face or limb anomalies as a major feature
• LD26 – Syndromes with limb anomalies as a major feature
• LD27 – Syndromes with skin or mucosal anomalies as a major feature
• LD28 – Syndromes with connective tissue involvement as a major feature
• LD29 – Syndromes with obesity as a major feature
• LD2A – Malformative disorders of sex development
• LD2B – Syndromes with premature ageing appearance as a major feature
• LD2C – Overgrowth syndromes
• LD2D – Phakomatoses or hamartoneoplastic syndromes
• LD2E – Syndromes with structural anomalies due to inborn errors of metabolism
• LD2F – Syndromes with multiple structural anomalies, without predominant body system involvement
• LD2G – Conjoined twins
• LD2H – Syndromic genetic deafness
• LD2Y – Other specified multiple developmental anomalies or syndromes
• LD2Z – Multiple developmental anomalies or syndromes, unspecified

Foundation entity

Syndromes with skeletal anomalies as a major feature – http://id.who.int/icd/entity/1496140949

Allowed postcoordination axes

• laterality
• specificAnatomy