LD24.HICD-11 MMS 2026-01
Dysostoses with predominant vertebral and costal involvement
Description
Any syndrome characterised by malformation of the musculoskeletal system during the antenatal period, which includes dysgenesis of the vertebrae and intercostal cartilage.
Index terms
- Dysostoses with predominant vertebral and costal involvement
- Spondylocostal dysostosis, autosomal dominant
- Spondylocostal dysostosis, autosomal recessive
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- Cerebrocostomandibular syndrome
- Cerebrofaciothoracic dysplasia
- Frontonasal dysplasia - Klippel-Feil syndrome
- Lumbar malsegmentation - short stature
- Dwarfism - tall vertebrae
- Syndromic progressive noninfectious anterior vertebral fusion
- Ankylosing vertebral hyperostosis with tylosis
- Ischio-vertebral syndrome
- Melhem-Fahl syndrome
Excludes
LD2F.1Y– Spondylocostal dysostosis - anal and genitourinary malformations
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.E– Bone dysplasias with multiple joint dislocationsLD24.F– Progressive ossification of skin, skeletal muscle, fascia, tendons or ligamentsLD24.G– Syndromic craniosynostosesLD24.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
Dysostoses with predominant vertebral and costal involvement – http://id.who.int/icd/entity/395969787
Part of: LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies