Q89.8 is the ICD-10 code for Other specified congenital malformations. It is a four-character subcategory of Q89 (Other congenital malformations, not elsewhere classified), 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
Q89.8 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
Q89.8Andra specificerade medfödda missbildningar
- Q89.8AAutosomalt dominant missbildning som ej klassificeras på annan plats
- Q89.8BAutosomalt recessiv missbildning som ej klassificeras på annan plats
- Q89.8CKönsbunden recessiv missbildning som ej klassificeras på annan plats
- Q89.8DMedfödd cysta som ej klassificeras på annan plats
- Q89.8ECentrofacial lentiginos
- Q89.8FKutan lentiginos med förmaksmyxom
- Q89.8GMultiple lentigines syndrome
- Q89.8WAndra specificerade medfödda missbildningar
Q89.8Annen spesifisert medfødt misdannelse
DQ898Anden medfødt misdannelse
- DQ898AHemigigantismus congenitus
- DQ898BHemihypertrophia congenita
- DQ898TTumor hos foster UNS
Q89.8Muut määritetyt synnynnäiset epämuodostumat
- Q89.80Kaudaalinen dysplasia sekvenssi
- Q89.88Muu synnynnäinen epämuodostuma
Q89.8Sonstige näher bezeichnete angeborene Fehlbildungen
Q89.8Autres malformations congénitales précisées
Q89.8overige gespecificeerde congenitale misvormingen
Listed through more specific codes:
- Q89.81Kabuki syndrome
- Q89.89Other specified congenital malformations
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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