Multiple epiphyseal dysplasia or pseudoachondroplasia

Child codes

• LD24.60 – Pseudoachondroplasia
• LD24.61 – Multiple epiphyseal dysplasias
• LD24.6Y – Other specified multiple epiphyseal dysplasia or pseudoachondroplasia

Sibling 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
• LD24.7 – 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 entity

Multiple epiphyseal dysplasia or pseudoachondroplasia – http://id.who.int/icd/entity/2078345611