Q39.8 is the ICD-10 code for Other congenital malformations of oesophagus. It is a four-character subcategory of Q39 (Congenital malformations of oesophagus), the most specific level in the WHO edition. It belongs to the block Q38–Q45 (Other congenital malformations of the digestive system) 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 Q39.8 includes
Conditions and terms that are coded here.
- Absent
- (of) oesophagus
- Congenital displacement
- (of) oesophagus
- Duplication
- (of) oesophagus
Q39.8 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
Q39.8Andra specificerade medfödda missbildningar av esofagus
Q39.8Annen spesifisert medfødt misdannelse i spiserør
DQ398Anden medfødt misdannelse i øsofagus
- DQ398AØsofagusagenesi
- DQ398BBrachyøsofagus
- DQ398CDislocatio congenita oesophagi
- DQ398DDuplikation af øsofagus
- DQ398EMedfødt øsofagusfistel
- DQ398FMedfødt øsofagushypoplasi
- DQ398GMedfødt megaøsofagus
Listed through more specific codes:
- Q39.80Kahdentunut ruokatorvi
- Q39.81Synnynnäinen ruokatorven liikehäiriö
- Q39.88Muu synnynnäinen ruokatorven epämuodostuma
Q39.8Sonstige angeborene Fehlbildungen des Ösophagus
Q39.8Autres malformations congénitales de l'œsophage
Q39.8overige gespecificeerde congenitale misvormingen van oesofagus
Q39.8Other congenital malformations of esophagus
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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