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ICD-10 diagnosis code

O28.5 Abnormal chromosomal and genetic finding on antenatal screening of mother

This page in Swedish

O28.5 is the ICD-10 code for Abnormal chromosomal and genetic finding on antenatal screening of mother. It is a four-character subcategory of O28 (Abnormal findings on antenatal screening of mother), the most specific level in the WHO edition. It belongs to the block O20–O29 (Other maternal disorders predominantly related to pregnancy) in Chapter XV, Pregnancy, childbirth and the puerperium.

Code type
Subcategory (4 characters)
Chapter
XV · O00–O99
Classification
WHO ICD-10, 2019 version

O28.5 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

O28.5Onormalt kromosomfynd och genetiskt fynd vid undersökning under graviditet

NorwayICD-10-NO

O28.5Unormalt kromosomfunn eller genetisk funn ved screening av mor under svangerskap

DenmarkICD-10-DK

DO285Abnormt fund i kromosomer eller gener hos moder ved graviditet

  • DO285AAbnormt fund i kromosomer hos moder ved graviditet
  • DO285BAbnormt fund i gener hos moder ved graviditet
FinlandICD-10-FI

O28.5Poikkeava kromosomilöydös tai muu geneettinen löydös synnytystä edeltävässä äidin terveystarkastuksessa

GermanyICD-10-GM

O28.5Abnormer Chromosomen- oder genetischer Befund bei der pränatalen Screeninguntersuchung der Mutter

FranceICD-10-FR

O28.5Résultats chromosomiques et génétiques anormaux au cours de l'examen prénatal

NetherlandsICD-10-NL

O28.5afwijkende chromosomale- en genetische-bevindingen bij prenatale

United StatesICD-10-CM

O28.5Abnormal chromosomal and genetic finding on antenatal screening of mother

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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