LD24
category
Syndromes with skeletal anomalies as a major feature
22 subordinate 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 density4B4YOther specified diseases of the immune system4B4ZDiseases of the immune system, unspecified
Nearby in Multiple developmental anomalies or syndromes
LD20Syndromes with central nervous system anomalies as a major featureLD21Syndromes with eye anomalies as a major featureLD22Syndromes with dental anomalies as a major featureLD23Syndromes with vascular anomalies as a major featureLD25Syndromes with face or limb anomalies as a major featureLD26Syndromes with limb anomalies as a major featureLD27Syndromes with skin or mucosal anomalies as a major featureLD28Syndromes with connective tissue involvement as a major feature