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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