LD24.EICD-11 MMS 2026-01
Bone dysplasias with multiple joint dislocations
Description
Any syndrome characterised by malformation of the musculoskeletal system during the antenatal period, which includes the dislocations of multiple joints.
Index terms
- Bone dysplasias with multiple joint dislocations
- Desbuquois syndrome
- Pseudodiastrophic dysplasia
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- Larsen syndrome
- Atelosteogenesis type I
- Atelosteogenesis type III
- Boomerang dysplasia
- Auriculo-osteodysplasia
- Auriculoosteodysplasia
- Coxoauricular syndrome
- Lethal Larsen-like syndrome
- Larsen-like osseous dysplasia - short stature
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LD24.0– Syndromes with micromeliaLD24.1– Bone diseases with increased bone densityLD24.2– Bone diseases with disorganised development of skeletal componentsLD24.3– Spondyloepiphyseal or spondyloepimetaphyseal dysplasiasLD24.4– Spondylometaphyseal dysplasiasLD24.5– Spondylodysplastic dysplasiasLD24.6– Multiple epiphyseal dysplasia or pseudoachondroplasiaLD24.7– Multiple metaphyseal dysplasiasLD24.8– Acromelic dysplasiasLD24.9– Acromesomelic dysplasiasLD24.A– Mesomelic or rhizomesomelic dysplasiasLD24.B– Short rib syndromesLD24.C– Bent bone dysplasiasLD24.D– Slender bone dysplasiasLD24.F– Progressive ossification of skin, skeletal muscle, fascia, tendons or ligamentsLD24.G– Syndromic craniosynostosesLD24.H– Dysostoses with predominant vertebral and costal involvementLD24.J– Patellar dysostosesLD24.K– Genetic bone diseases with decreased bone densityLD24.Y– Other specified syndromes with skeletal anomalies as a major featureLD24.Z– Syndromes with skeletal anomalies as a major feature, unspecified
Foundation entity
Bone dysplasias with multiple joint dislocations – http://id.who.int/icd/entity/689620137
Allowed postcoordination axes
Part of: LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies