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ICD-10 diagnosis code

Q87.0 Congenital malformation syndromes predominantly affecting facial appearance

This page in Swedish

Q87.0 is the ICD-10 code for Congenital malformation syndromes predominantly affecting facial appearance. 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 Q87.0 includes

Conditions and terms that are coded here.

  • Acrocephalopolysyndactyly
  • Acrocephalosyndactyly [Apert]
  • Cryptophthalmos syndrome
  • Cyclopia
  • Syndrome:
    • Goldenhar
    • Moebius
    • oro-facial-digital
    • Robin
  • Whistling face

Q87.0 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

Q87.0Medfödda missbildningssyndrom som främst påverkar ansiktets utseende

  • Q87.0AAkrocefalopolysyndaktyli
  • Q87.0BAkrocefalosyndaktyli [Apert]
  • Q87.0CCyklopi
  • Q87.0DGoldenhars syndrom
  • Q87.0ERobins syndrom
  • Q87.0GOrofacialdigitalt syndrom I
  • Q87.0JDyscephalia mandibulo-oculofacialis
  • Q87.0KFamiljär mandibuloakral dysplasi
  • and 4 more national subcodes
NorwayICD-10-NO

Q87.0Medfødt misdannelsessyndrom som hovedsaklig påvirker ansiktets utseende

DenmarkICD-10-DK

DQ870Syndromer med medfødte misdannelser overvejende i ansigtet

  • DQ870AAkrocefalopolysyndaktyli
  • DQ870BAkrocefalosyndaktyli type 1
  • DQ870CKryptoftalmi
  • DQ870DKyklopi
  • DQ870FOkulo-aurikulo-vertebral dysplasi
  • DQ870GMöbius' syndrom
  • DQ870HOro-facio-digitalt syndrom
  • DQ870IPierre Robins syndrom
  • and 2 more national subcodes
FinlandICD-10-FI

Q87.0Etenkin kasvojen ulkonäköön vaikuttavat synnynnäiset epämuodostumaoireyhtymät

  • Q87.00Treacher-Collins oireyhtymä
  • Q87.01Akrokefalosyndaktylia (Apert)
  • Q87.02Akrokefalopolysyndaktylia
  • Q87.03Goldenhaarin oireyhtymä
  • Q87.04(Pierre-)Robinin sekvenssi
  • Q87.05Möbiuksen oireyhtymä (aivohermojen liiketumakkeiden vajaakehitys)
  • Q87.06Velokardiofakiaalinen oireyhtymä
  • Q87.09Muu etenkin kasvojen ulkonäköön vaikuttava synnynnäinen epämuodostumaoireyhtymä
GermanyICD-10-GM

Q87.0Angeborene Fehlbildungssyndrome mit vorwiegender Beteiligung des Gesichtes

FranceICD-10-FR

Q87.0Syndromes congénitaux malformatifs atteignant principalement l'aspect de la face

NetherlandsICD-10-NL

Q87.0congenitale gestoorde ontwikkelingssyndromen waarbij voornamelijk

United StatesICD-10-CM

Q87.0Congenital malformation syndromes predominantly affecting facial appearance

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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