Syndromes with limb anomalies as a major feature

Child codes

• LD26.0 – Combined reduction defects of upper and lower limbs
• LD26.1 – Complex brachydactylies
• LD26.2 – Syndromes with limb duplication, polydactyly, syndactyly or triphalangism
• LD26.3 – Syndromes with synostoses of limbs
• LD26.4 – Arthrogryposis syndromes
• LD26.5 – Constriction rings
• LD26.6 – Congenital vascular bone syndromes
• LD26.Y – Other specified syndromes with limb anomalies as a major feature
• LD26.Z – Syndromes with limb anomalies as a major feature, unspecified

Sibling codes

• LD20 – Syndromes with central nervous system anomalies as a major feature
• LD21 – Syndromes with eye anomalies as a major feature
• LD22 – Syndromes with dental anomalies as a major feature
• LD23 – Syndromes with vascular anomalies as a major feature
• LD24 – Syndromes with skeletal anomalies as a major feature
• LD25 – Syndromes with face or limb anomalies as a major feature
• LD27 – Syndromes with skin or mucosal anomalies as a major feature
• LD28 – Syndromes with connective tissue involvement as a major feature
• LD29 – Syndromes with obesity as a major feature
• LD2A – Malformative disorders of sex development
• LD2B – Syndromes with premature ageing appearance as a major feature
• LD2C – Overgrowth syndromes
• LD2D – Phakomatoses or hamartoneoplastic syndromes
• LD2E – Syndromes with structural anomalies due to inborn errors of metabolism
• LD2F – Syndromes with multiple structural anomalies, without predominant body system involvement
• LD2G – Conjoined twins
• LD2H – Syndromic genetic deafness
• LD2Y – Other specified multiple developmental anomalies or syndromes
• LD2Z – Multiple developmental anomalies or syndromes, unspecified

Foundation entity

Syndromes with limb anomalies as a major feature – http://id.who.int/icd/entity/415035569

Allowed postcoordination axes

• laterality
• specificAnatomy