Q39.8
BillableOther congenital malformations of esophagus
Other congenital malformations of esophagus
Status
Billable / Specific
Parent Code
Q39Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital absence of esophagus
- Congenital displacement of esophagus
- Congenital duplication of esophagus
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- CDH - Congenital diaphragmatic hernia17190001
- Congenital diaphragmatic hernia17190001
- Absent esophagus36376006
- Absent oesophagus36376006
- Congenital absence of esophagus36376006
- Congenital absence of oesophagus36376006
- Compression of esophagus39392002
- Compression of oesophagus39392002
- Vascular compression of esophagus by aberrant artery53190001
- Vascular compression of oesophagus by aberrant artery53190001
- Congenital duplication of esophagus66865009
- Congenital duplication of oesophagus66865009
- Esophageal duplication66865009
- Oesophageal duplication66865009
- Cardio-esophageal relaxation70257007
- Cardiochalasia70257007
- Chalasia of cardia70257007
- Chalasia of lower esophageal sphincter70257007
- Chalasia of lower oesophageal sphincter70257007
- Hypotensive lower esophageal sphincter70257007
- Hypotensive lower oesophageal sphincter70257007
- Neuhauser-Berenberg syndrome70257007
- Relaxation of lower esophageal sphincter70257007
- Relaxation of lower oesophageal sphincter70257007
- Congenital displacement of esophagus79510004
- Congenital displacement of oesophagus79510004
- Congenital malposition of esophagus79510004
- Congenital malposition of oesophagus79510004
- Congenital malpositioned esophagus79510004
- Congenital malpositioned oesophagus79510004
- Congenital cyst of esophagus87047005
- Congenital cyst of oesophagus87047005
- Congenital displacement of stomach89378007
- Congenital malposition of stomach89378007
- Congenital malpositioned stomach89378007
- Congenital tubular duplication of esophagus716280004
- Congenital tubular duplication of oesophagus716280004
- Congenital chalasia of esophagus721154006
- Congenital chalasia of oesophagus721154006
- Congenital short esophagus721155007
- Congenital short oesophagus721155007
- Duplication cyst of esophagus721161005
- Esophageal duplication cyst721161005
- Oesophageal duplication cyst721161005
- Angioectopia783409001
- Ectopic artery783409001
- Agenesis of esophagus1003569002
- Agenesis of oesophagus1003569002
- Congenital brachyesophagus, intrathoracic stomach, vertebral anomalies syndrome1197754004
- Congenital brachyoesophagus, intrathoracic stomach, vertebral anomalies syndrome1197754004
- Serpentine-like syndrome1197754004
UMLS
- Absent esophagusC0266127
- Absent oesophagusC0266127
- Agenesis of esophagusC0266127
- Agenesis of esophagus (disorder)C0266127
- Agenesis of oesophagusC0266127
- Congenital absence of esophagusC0266127
- Congenital absence of esophagus (disorder)C0266127
- Congenital absence of oesophagusC0266127
- Congenital displacement of esophagusC0266132
- Congenital displacement of esophagus (disorder)C0266132
- Congenital displacement of oesophagusC0266132
- Congenital malposition of esophagusC0266132
- Congenital malposition of oesophagusC0266132
- Congenital malpositioned esophagusC0266132
- Congenital malpositioned oesophagusC0266132
- Congenital duplication of esophagusC0266135
- Congenital duplication of esophagus (disorder)C0266135
- Congenital duplication of oesophagusC0266135
- Esophageal DuplicationC0266135
- Esophageal duplicationC0266135
- Oesophageal duplicationC0266135
- Other congenital malformations of esophagusC0478028
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of esophagus?
The ICD-10-CM code for other congenital malformations of esophagus is Q39.8. The full clinical description is "Other congenital malformations of esophagus". Q39.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q39.8 mean?
ICD-10-CM code Q39.8 represents "Other congenital malformations of esophagus". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q39.8 a billable code?
Yes, Q39.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q39.8 in?
Q39.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q39.8 map to?
Q39.8 maps to 16 SNOMED CT concepts: 36376006, 1003569002, 783409001, 17190001, 70257007, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q39.8?
Q39.8 is linked to 4 UMLS Concept Unique Identifiers: C0266127, C0266132, C0266135, C0478028. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.