ICD-10 diagnosis code

Z82.7 Family history of congenital malformations, deformations and chromosomal abnormalities

This page in Swedish

Z82.7 is the ICD-10 code for Family history of congenital malformations, deformations and chromosomal abnormalities. It is a four-character subcategory of Z82 (Family history of certain disabilities and chronic diseases leading to disablement), the most specific level in the WHO edition. It belongs to the block Z80–Z99 (Persons with potential health hazards related to family and personal history and certain conditions influencing health status) in Chapter XXI, Factors influencing health status and contact with health services.

Code type
Subcategory (4 characters)
Chapter
XXI · Z00–Z99
Classification
WHO ICD-10, 2019 version

What Z82.7 includes

Conditions and terms that are coded here.

Z82.7 in national editions

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

NorwayICD-10-NO

Z82.7Opplysning om medfødte misdannelse, deformitet eller kromosomavvik i familieanamnesen

DenmarkICD-10-DK

DZ827Familieanamnese med misdannelser eller kromosomabnormiteter

FinlandICD-10-FI

Z82.7Synnynnäisten epämuodostumien, epämuotoisuuksien tai kromosomipoikkeavuuksien esiintyminen suvussa

FranceICD-10-FR

Z82.7Antécédents familiaux de malformations congénitales et anomalies

NetherlandsICD-10-NL

Z82.7familieanamnese met congenitale afwijkingen, misvormingen en

United StatesICD-10-CM

Listed through more specific codes:

  • Z82.71Family history of polycystic kidney
  • Z82.79Family history of other congenital malformations, deformations and chromosomal abnormalities

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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