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ICD-10 diagnosis code

Q87.2 Congenital malformation syndromes predominantly involving limbs

This page in Swedish

Q87.2 is the ICD-10 code for Congenital malformation syndromes predominantly involving limbs. It is a four-character subcategory of Q87 (Other specified congenital malformation syndromes affecting multiple systems), the most specific level in the WHO edition. It belongs to the block Q80–Q89 (Other congenital malformations) in Chapter XVII, Congenital malformations, deformations and chromosomal abnormalities.

Code type
Subcategory (4 characters)
Chapter
XVII · Q00–Q99
Classification
WHO ICD-10, 2019 version

What Q87.2 includes

Conditions and terms that are coded here.

  • Syndrome:
    • Holt-Oram
    • Klippel-Trénaunay-Weber
    • nail patella
    • Rubinstein-Taybi
    • sirenomelia
    • thrombocytopenia with absent radius [TAR]
    • VATER

Q87.2 in national editions

Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.

SwedenICD-10-SE

Q87.2Medfödda missbildningssyndrom som främst engagerar extremiteter

  • Q87.2BKlippel-Trénaunay-Webers syndrom
  • Q87.2CNail patella syndrome
  • Q87.2DRubinstein-Taybis syndrom
  • Q87.2WAndra medfödda missbildningssyndrom som främst engagerar extremiteter
NorwayICD-10-NO

Q87.2Medfødt misdannelsessyndrom som hovedsaklig omfatter ekstremiteter

DenmarkICD-10-DK

DQ872Syndromer med medfødte misdannelser overvejende i ekstremiteter

  • DQ872AAtriodigital syndrom
  • DQ872BKlippel-Trenaunay-Webers syndrom
  • DQ872CNegl-patella-syndrom
  • DQ872DRubinstein-Taybis syndrom
  • DQ872ESirenomeli
  • DQ872FTrombocytopeni med aplasi af radius
  • DQ872GVACTERL syndrom
FinlandICD-10-FI

Q87.2Etenkin raajoihin vaikuttavat synnynnäiset epämuodostumaoireyhtymät

  • Q87.20Holt-Oramin oireyhtymä
  • Q87.21Klippel-Trénaunay-Weberin oireyhtymä
  • Q87.22Nail-patella-oireyhtymä
  • Q87.23Rubinstein-Taybin oireyhtymä
  • Q87.24Sirenomelia
  • Q87.25Trombosytopenia ja värttinäluun puuttuminen (TAR-oireyhtymä)
  • Q87.26VATER-assosiaatio
  • Q87.27CHARGE-assosiaatio
  • and 1 more national subcodes
GermanyICD-10-GM

Q87.2Angeborene Fehlbildungssyndrome mit vorwiegender Beteiligung der Extremitäten

FranceICD-10-FR

Q87.2Syndromes congénitaux malformatifs impliquant principalement les membres

NetherlandsICD-10-NL

Q87.2congenitale gestoorde ontwikkelingssyndromen van hoofdzakelijk

United StatesICD-10-CM

Q87.2Congenital malformation syndromes predominantly involving limbs

Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.

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