LD24.DICD-11 MMS 2026-01
Slender bone dysplasias
Description
Any syndrome characterised by dwarfism, thin bones, multiple fractures, and prenatal or early postnatal death.
Index terms
- Slender bone dysplasias
- 3M syndrome
- Kenny-Caffey syndrome, autosomal dominant
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- Kenny-Caffey syndrome, autosomal recessive
- Sanjad-Sakati syndrome
- Hypoparathyroidism - intellectual deficit - dysmorphism
- Hypoparathyroidism - short stature - intellectual deficit - seizures
- Osteocraniostenosis
- Seckel syndrome
- Dwarfism - thin bones - multiple fractures
- Microcephalic primordial dwarfism, Toriello type
- Microcephalic osteodysplastic dysplasia, Saul-Wilson type
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.E– Bone dysplasias with multiple joint dislocationsLD24.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
Slender bone dysplasias – http://id.who.int/icd/entity/691657602
Allowed postcoordination axes
Part of: LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies