Docdemic

ICD-10 diagnosis code

Q91.0 Trisomy 18, meiotic nondisjunction

This page in Swedish

Q91.0 is the ICD-10 code for Trisomy 18, meiotic nondisjunction. It is a four-character subcategory of Q91 (Edwards syndrome and Patau syndrome), the most specific level in the WHO edition. It belongs to the block Q90–Q99 (Chromosomal abnormalities, not elsewhere classified) in Chapter XVII, Congenital malformations, deformations and chromosomal abnormalities.

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

Q91.0 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

Q91.0Trisomi 18, meiotisk nondisjunction

NorwayICD-10-NO

Q91.0Trisomi 18, meiotisk nondisjunksjon

DenmarkICD-10-DK

DQ910Trisomi 18, meiotisk nondisjunktion

  • DQ910ATrisomi 17-18, meiotisk nondisjunktion
FinlandICD-10-FI

Q91.0Trisomia 18, meioottinen nondisjunktio

GermanyICD-10-GM

Q91.0Trisomie 18, meiotische Non-disjunction

FranceICD-10-FR

Q91.0Trisomie 18, non-disjonction méïotique

NetherlandsICD-10-NL

Q91.0trisomie 18, meiotische non-disjunctie

United StatesICD-10-CM

Q91.0Trisomy 18, nonmosaicism (meiotic nondisjunction)

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.

Look up another code

Stop looking codes up by hand

Docdemic listens to the consultation, writes the note and suggests the diagnosis and procedure codes that fit it, each one checked against your country’s official code list.

Try Docdemic free