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

From Embryology
mNo edit summary
mNo edit summary
Line 43: Line 43:
   
   
* LD2Z Multiple developmental anomalies or syndromes, unspecified
* LD2Z Multiple developmental anomalies or syndromes, unspecified
|}
|}<noinclude>[[Category:Template]][[Category:Abnormal Development]][[Category:Table]][[Category:ICD-11]][[Category:2018]][[Category:Draft]]</noinclude>

Revision as of 11:49, 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