World Health Organization · 2026-01 · English
LD24 Syndromes with skeletal anomalies as a major feature
Official WHO ICD-11 MMS tabulation. This international classification is separate from US ICD-10-CM. For complete instructions and postcoordination, consult the WHO browser.
More specific codes
LD24.0Syndromes with micromeliaLD24.1Bone diseases with increased bone densityLD24.2Bone diseases with disorganised development of skeletal componentsLD24.3Spondyloepiphyseal or spondyloepimetaphyseal dysplasiasLD24.4Spondylometaphyseal dysplasiasLD24.5Spondylodysplastic dysplasiasLD24.6Multiple epiphyseal dysplasia or pseudoachondroplasiaLD24.7Multiple metaphyseal dysplasiasLD24.8Acromelic dysplasiasLD24.9Acromesomelic dysplasiasLD24.AMesomelic or rhizomesomelic dysplasiasLD24.BShort rib syndromesLD24.CBent bone dysplasiasLD24.DSlender bone dysplasiasLD24.EBone dysplasias with multiple joint dislocationsLD24.FProgressive ossification of skin, skeletal muscle, fascia, tendons or ligamentsLD24.GSyndromic craniosynostosesLD24.HDysostoses with predominant vertebral and costal involvementLD24.JPatellar dysostosesLD24.KGenetic bone diseases with decreased bone densityLD24.YOther specified syndromes with skeletal anomalies as a major featureLD24.ZSyndromes with skeletal anomalies as a major feature, unspecified© World Health Organization · CC BY-ND 3.0 IGO