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  
  • 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