Catalog
Multiple developmental anomalies or syndromes
No MMS code
Link to WHO Definition
Multiple developmental anomalies or syndromes – http://id.who.int/icd/entity/770439884
Complex developmental anomalies involving more than one body system
Parents
Children
- LD22 Syndromes with dental anomalies as a major feature
- LD28 Syndromes with connective tissue involvement as a major feature
- LD25 Syndromes with face or limb anomalies as a major feature
- LD2D Phakomatoses or hamartoneoplastic syndromes
- LD24 Syndromes with skeletal anomalies as a major feature
- LD2B Syndromes with premature ageing appearance as a major feature
- LD2G Conjoined twins
- LD23 Syndromes with vascular anomalies as a major feature
- LD20 Syndromes with central nervous system anomalies as a major feature
- LD27 Syndromes with skin or mucosal anomalies as a major feature
- LD2H Syndromic genetic deafness
- LD2F Syndromes with multiple structural anomalies, without predominant body system involvement
- LD2C Overgrowth syndromes
- LD26 Syndromes with limb anomalies as a major feature
- LD29 Syndromes with obesity as a major feature
- LD2A Malformative disorders of sex development
- LD21 Syndromes with eye anomalies as a major feature
- LD2E Syndromes with structural anomalies due to inborn errors of metabolism