Template:ICD-11-Multiple developmental anomalies or syndromes table: Difference between revisions
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Multiple developmental anomalies or syndromes | ! [[International Classification of Diseases|ICD-11]] Multiple developmental anomalies or syndromes | ||
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LD20 Syndromes with central nervous system anomalies as a major feature | * LD20 Syndromes with central nervous system anomalies as a major feature | ||
LD21 Syndromes with eye anomalies as a major feature | * LD21 Syndromes with eye anomalies as a major feature | ||
LD22 Syndromes with dental anomalies as a major feature | * LD22 Syndromes with dental anomalies as a major feature | ||
LD23 Syndromes with vascular anomalies as a major feature | * LD23 Syndromes with vascular anomalies as a major feature | ||
LD24 Syndromes with skeletal 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 | * LD25 Syndromes with face or limb anomalies as a major feature | ||
LD26 Syndromes with limb anomalies as a major feature | * LD26 Syndromes with limb anomalies as a major feature | ||
LD27 Syndromes with skin or mucosal 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 | * LD28 Syndromes with connective tissue involvement as a major feature | ||
LD29 Syndromes with obesity as a major feature | * LD29 Syndromes with obesity as a major feature | ||
LD2A Malformative disorders of sex development | * LD2A Malformative disorders of sex development | ||
LD2B Syndromes with premature ageing appearance as a major feature | * LD2B Syndromes with premature ageing appearance as a major feature | ||
LD2C Overgrowth syndromes | * LD2C Overgrowth syndromes | ||
LD2D Phakomatoses or hamartoneoplastic syndromes | * LD2D Phakomatoses or hamartoneoplastic syndromes | ||
LD2E Syndromes with structural anomalies due to inborn errors of metabolism | * LD2E Syndromes with structural anomalies due to inborn errors of metabolism | ||
LD2F Syndromes with multiple structural anomalies, without predominant body system involvement | * LD2F Syndromes with multiple structural anomalies, without predominant body system involvement | ||
LD2G Conjoined twins | * LD2G Conjoined twins | ||
LD2H Syndromic genetic deafness | * LD2H Syndromic genetic deafness | ||
LD2Y Other specified multiple developmental anomalies or syndromes | * LD2Y Other specified multiple developmental anomalies or syndromes | ||
LD2Z Multiple developmental anomalies or syndromes, unspecified | * LD2Z Multiple developmental anomalies or syndromes, unspecified | ||
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Revision as of 11:48, 24 June 2018
ICD-11 Multiple developmental anomalies or syndromes |
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