Multiple developmental anomalies or syndromes

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Complex developmental anomalies involving more than one body system

sections/codes in this section (LD20-LD2Z)

• Syndromes with central nervous system anomalies as a major feature  (LD20)
• Syndromes with eye anomalies as a major feature  (LD21)
• Syndromes with dental anomalies as a major feature  (LD22)
• Syndromes with vascular anomalies as a major feature  (LD23)
• Syndromes with skeletal anomalies as a major feature  (LD24)
• Syndromes with face or limb anomalies as a major feature  (LD25)
• Syndromes with limb anomalies as a major feature  (LD26)
• Syndromes with skin or mucosal anomalies as a major feature  (LD27)
• Syndromes with connective tissue involvement as a major feature  (LD28)
• Syndromes with obesity as a major feature  (LD29)
• Malformative disorders of sex development  (LD2A)
• Syndromes with premature ageing appearance as a major feature  (LD2B)
• Overgrowth syndromes  (LD2C)
• Phakomatoses or hamartoneoplastic syndromes  (LD2D)
• Syndromes with structural anomalies due to inborn errors of metabolism  (LD2E)
• Syndromes with multiple structural anomalies, without predominant body system involvement  (LD2F)
• Conjoined twins  (LD2G)
• Syndromic genetic deafness  (LD2H)
• Other specified multiple developmental anomalies or syndromes  (LD2Y)
• Multiple developmental anomalies or syndromes, unspecified  (LD2Z)

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