BlockL1-LD2Level 2

Multiple developmental anomalies or syndromes

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LD20Syndromes with central nervous system anomalies as a major feature

LD21Syndromes with eye anomalies as a major feature

LD22Syndromes with dental anomalies as a major feature

LD23Syndromes with vascular anomalies as a major feature

LD24Syndromes with skeletal anomalies as a major feature

LD25Syndromes with face or limb anomalies as a major feature

LD26Syndromes with limb anomalies as a major feature

LD27Syndromes with skin or mucosal anomalies as a major feature

LD28Syndromes with connective tissue involvement as a major feature

LD29Syndromes with obesity as a major feature

LD2AMalformative disorders of sex development

LD2BSyndromes with premature ageing appearance as a major feature

LD2COvergrowth syndromes

LD2DPhakomatoses or hamartoneoplastic syndromes

LD2ESyndromes with structural anomalies due to inborn errors of metabolism

LD2FSyndromes with multiple structural anomalies, without predominant body system involvement

LD2GConjoined twins

LD2HSyndromic genetic deafness

LD2YOther specified multiple developmental anomalies or syndromes

LD2ZMultiple developmental anomalies or syndromes, unspecified

No cross-system equivalences mapped for this node.