Template:ICD-11-Multiple developmental anomalies or syndromes table: Difference between revisions

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* LD2H Syndromic genetic deafness   
* LD2H Syndromic genetic deafness   
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| LD2Y Other specified multiple developmental anomalies or syndromes 
   
   
* LD2Y Other specified multiple developmental anomalies or syndromes 
LD2Z Multiple developmental anomalies or syndromes, unspecified
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* LD2Z Multiple developmental anomalies or syndromes, unspecified
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Latest revision as of 13:11, 24 June 2018

ICD-11 Multiple developmental anomalies or syndromes  
  • LD20 Syndromes with central nervous system anomalies as a major feature
  • LD21 Syndromes with eye anomalies as a major feature
  • LD22 Syndromes with dental anomalies as a major feature
  • LD23 Syndromes with vascular 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
  • LD26 Syndromes with limb 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
  • LD29 Syndromes with obesity as a major feature
  • LD2A Malformative disorders of sex development
  • LD2B Syndromes with premature ageing appearance as a major feature
  • LD2C Overgrowth syndromes
  • LD2D Phakomatoses or hamartoneoplastic syndromes
  • LD2E Syndromes with structural anomalies due to inborn errors of metabolism
  • LD2F Syndromes with multiple structural anomalies, without predominant body system involvement
  • LD2G Conjoined twins
  • LD2H Syndromic genetic deafness
LD2Y Other specified multiple developmental anomalies or syndromes

LD2Z Multiple developmental anomalies or syndromes, unspecified

ICD-11 Links:  ICD-11 | Anomalies one body system | Multiple anomalies or syndromes | Chromosomal anomalies | Intellectual development | Abnormal Development | Prenatal Diagnosis | Birth | Neonatal Diagnosis | ICD-10 | Reports | | Category:ICD-11